Process for preparing GIP / GLP1 dual agonists

Abstract

To provide novel intermediates and processes useful in the manufacture of tirzepatide, a GIP / GLP1 dual agonist, or a pharmaceutically acceptable salt thereof.SOLUTION: The present invention provides a plurality of peptide derivatives having a specific sequence and structure as an intermediate useful in the manufacture of tirzepatide, or a pharmaceutically acceptable salt thereof, and a process for coupling with the intermediate bound to resin and deprotecting.SELECTED DRAWING: None

Description

Detailed Description of the Invention

[0001] The present invention provides processes and intermediates for making the GIP / GLP1 dual agonist peptide, tirzepatide, or a pharma- ceutically acceptable salt thereof.

[0002] Diabetes is a chronic disease characterized by hyperglycemia due to defects in insulin secretion, insulin action, or both. In type 2 diabetes ("T2D"), the combined effects of insulin secretion deficiency and insulin resistance are associated with elevated blood glucose levels. Tirzepatide, a GIP / GLP1 dual agonist, is described and claimed in U.S. Patent No. 9,474,780 ("the '780 patent"). Tirzepatide may be useful in the treatment of T2D.

[0003] US9474780 generally describes peptides and methods for making GIP / GLP1 dual agonists.

[0004] Processes and intermediates are needed to enable improved techniques for the production of tirzepatide with a combination of advantages, including commercially desirable purity. Similarly, efficient and environmentally "green" processes are needed, including stable intermediates to provide tirzepatide with fewer purification steps. Improved technologies are also needed to provide tirzepatide manufacturing processes that minimize waste streams to enhance both environmental and operator safety. Large-scale preparation of pharmaceutical superior tirzepatide presents several technical challenges that can affect overall yield and purity. Processes are needed to avoid the use of transition metals and / or harsh reaction conditions that are incompatible with peptide synthesis.

[0005] The present invention seeks to meet these needs by providing novel intermediates and processes useful for the production of tirzepatide (SEQ ID NO: 1), or a pharma- ceutically acceptable salt thereof. The improved tirzepatide production process of the present invention provides intermediates and process reactions that embody a combination of advances, including an efficient route with fewer steps, while maintaining high quality and purity. Importantly, the improved processes and intermediates reduce resource intensity and minimize waste streams.

[0006] The improved process described herein provides various embodiments of intermediates useful in the production of tirzepitide.

[0007] The present invention provides a compound of SEQ ID NO: 17, or a pharma- ceutically acceptable salt thereof. The present invention provides a compound of SEQ ID NO: 11, or a pharma- ceutically acceptable salt thereof. The present invention provides a compound of SEQ ID NO: 22, or a pharma- ceutically acceptable salt thereof. The present invention provides a compound of SEQ ID NO: 21, or a pharma- ceutically acceptable salt thereof. The present invention provides a compound of SEQ ID NO: 20, or a pharma- ceutically acceptable salt thereof. The present invention provides a compound of SEQ ID NO: 2, or a pharma- ceutically acceptable salt thereof. The present invention provides a compound of SEQ ID NO: 4, or a pharma- ceutically acceptable salt thereof. The present invention provides a compound of SEQ ID NO: 7, or a pharma- ceutically acceptable salt thereof. The present invention provides a compound of SEQ ID NO: 14, or a pharma- ceutically acceptable salt thereof. The present invention provides a compound of SEQ ID NO: 33, or a pharma- ceutically acceptable salt thereof. The present invention provides a compound of SEQ ID NO: 32, or a pharma- ceutically acceptable salt thereof. The present invention provides a compound of SEQ ID NO: 34, or a pharma- ceutically acceptable salt thereof. The present invention provides a compound of SEQ ID NO: 35, or a pharma- ceutically acceptable salt thereof. The present invention provides a compound of SEQ ID NO: 36, or a pharma- ceutically acceptable salt thereof.The present invention provides a compound of SEQ ID NO: 38, or a pharma- ceutically acceptable salt thereof.The present invention provides a compound of SEQ ID NO: 39, or a pharma- ceutically acceptable salt thereof.

[0008] A compound of the formula: [ka] or a pharma- ceutically acceptable salt thereof.

[0009] A compound of the formula: [ka] or a pharma- ceutically acceptable salt thereof.

[0010] The present invention provides a process for preparing tirzepatide using nanofiltration.

[0011] The present invention provides a process for preparing tirzepatide, comprising deprotecting the compound of SEQ ID NO: 22, or a pharma- ceutically acceptable salt thereof.

[0012] A process for selectively acylating lysine amino acids and N-terminally protected lysine amino acids is provided. 2 With t-butyl-eicosanediyl-Glu-(O-tert-butyl)-(8-amino-3,6-dioxaoctanoic acid)-(8-amino-3,6-dioxaoctanoic acid)-OH) is provided. A process for preparing tirzepatide is provided, comprising deprotecting a compound of SEQ ID NO: 22 or a pharma- ceutically acceptable salt thereof.

[0013] A process for deprotecting tirzepatide is provided, wherein the deprotection solution comprises dithiothreitol, triisopropylsilane, and trifluoroacetic acid.

[0014] Resin-bound peptide-lysine-NH 2 is a compound of the formula: [ka] or a pharma- ceutically acceptable salt thereof.

[0015] A process for converting a depsipeptide isomer to a desired peptide is provided, comprising adjusting the pH of the depsipeptide isomer to between about pH 7 and about pH 10, and incubating the depsipeptide isomer at pH 7 to pH 10 for at least 1 hour.

[0016] A process for converting depsipeptide isomers is provided, in which the depsipeptide isomers are adjusted to a pH of about 8.5 to about pH 9.5.

[0017] A process for converting a depsipeptide isomer is provided, wherein the depsipeptide isomer is a compound of SEQ ID NO: 40, or a pharma- ceutically acceptable salt thereof.

[0018] Radical-based desulfurization is provided, comprising contacting a peptide with a radical initiator. In one embodiment, the desulfurization comprises contacting a peptide suitable for desulfurization with a water-soluble radical initiator. In one embodiment, the radical initiator is an azo initiator. In one embodiment, the radical initiator is selected from the group consisting of 2,2'-azobis[2-(2-imidazolin-2-yl)propane]dihydrochloride (VA-044) and 2,2'-azobis(2-methylpropionamidine)dihydrochloride (VA-050).

[0019] The radical-based desulfurization method provided herein is environmentally desirable, transition metal-free, and conditions compatible with peptide synthesis.

[0020] As used herein, the following abbreviations have the meanings set forth herein: "SPPS" means solid phase peptide synthesis, "Fmoc" means fluorenylmethyloxycarbonyl chloride, "Pip" means piperidine, "DIC" means diisopropylcarbodiimide, "Oxyma" means ethyl cyanohydroxyiminoacetate, "DCM" means dichloromethane, "IPA" means isopropanol, "MTBE" means methyl tert-butyl ether, and "TFA" means trifluoroacetic acid. "TIPS" means triisopropylsilane, "DTT" means dithiothreitol, "UPLC" means ultra-performance liquid chromatography, "HFIP" means hexafluoroisopropanol, "CTC" means chlorotrityl, "HATU" means (1-[bis(dimethylamino)methylene]-1H-1,2,3-triazolo[4,5-b]pyridinium 3-oxide hexafluorophosphate, "TFET" means 2,2,2-trifluoroethanethiol, and "DIEA" means N,N-diisopropyl ether. "AEEA" means 17-amino-10-oxo-3,6,12,15-tetraoxa-9-azaheptadecanoic acid, "TCEP" means tris(2-carboxyethyl)phosphine, "DCU" means dicyclohexylurea, "DCC" means dicyclohexylcarbodiimide, "TMSA" means trimethylsilylamide, "HOBt" means hydroxybenzotriazole, "HRMS" means high resolution mass spectrometry, "LPPS" means liquid phase peptide synthesis, and "MS "MPR" means mixed product mixing suspension reactor, "MPA" means mobile phase A, "MPB" means mobile phase B, "L-GSH" means L-glutathione reducing solution, "TZP" means tirzepatide, "AP" means active pharmaceutical ingredient, "API" means active pharmaceutical ingredient, "PyBOP" means (benzotriazol-1-yloxy)tripyrrolidinophosphonium hexafluorophosphate, "DEA" means diethylamine, "TBTU" means 2-(1H-benzotriazol-1-yl)-1,1,3,"PyClock" means 6-chloro-benzotriazol-1-yloxy-tris-pyrrolidinophosphonium hexafluorophosphate. As shown herein, one-letter abbreviations for amino acids are shown in boldface type, and atoms are shown as non-bold text, usually in a smaller font, to distinguish them from one-letter amino acid abbreviations. As used herein, when an amino acid abbreviation appears with a number above the amino acid, the number refers to the position of the corresponding amino acid in the final tirzepatide product. Numbers are provided for convenience, and the appearance or non-appearance of such numbers in a sequence does not affect the amino acid sequence or peptide shown in such sequence. As used herein, the term "protected" means that a protecting group is attached at the indicated position. Those skilled in the art will recognize that a variety of protecting groups are well known and that alternative protecting groups may be suitable for a particular process.

[0021] Those skilled in the art will understand that there are alternative resins for constructing the peptides presented herein.For example, Sieber amide resin and Rink amide resin are well known to those skilled in the art for preparing the peptides disclosed herein, but alternative resins may be selected for the preparation of the peptides described herein.For example, but not limited to, 2-CTC and related resins can be used to prepare the target peptide, followed by a C-terminal amidation step.

[0022] Solid phase peptide synthesis (SPPS) builds are achieved using standard fluorenylmethyloxycarbonyl chloride (Fmoc) peptide chemistry techniques utilizing sequential couplings with an automated peptide synthesizer. The resin is swollen in DMF and then deprotected using 20% ​​piperidine (Pip) / DMF (3x30 min). Subsequent Fmoc deprotections use 3x30 min treatments of 20% Pip / DMF, and for more difficult couplings, 4x30 min treatments are used. After deprotection, the resin is washed with 10 volumes of DMF washes for 5x2 min. Preactivation of amino acids uses a diisopropylcarbodiimide (DIC) / ethyl cyanohydroxyiminoacetate (Oxyma) DMF solution for 30 min at room temperature. Coupling of activated amino acids to the resin-bound peptide occurs for the time specified for each individual amino acid. Each coupling is followed by a solvent wash with 10 volumes of DMF for 5x2 min. To isolate the final product, the resin-bound product is washed with 10 volumes of DCM for 5x2 min to remove DMF. The resin is washed with 10 volumes of IPA for 2x2 min to remove DCM and with 10 volumes of methyl-tert-butyl ether (MTBE) for 5x2 min before drying the product in vacuum at 40°C. The resin-bound product is stored refrigerated (-20°C). For analysis, the peptide is purified by HPLC using trifluoroacetic acid (TFA) / H2O2 elution. 2 Cleavage from the resin using an acidic cocktail consisting of O / TIPS (triisopropylsilane) / DTT (dithiothreitol) in the following ratios (0.93v / 0.04v / 0.03v / 0.03w). Swell the resin in DCM (4-5mL, 3x30min) and drain. Add the cleavage cocktail (4-5mL) to the pre-swollen resin and stir the suspension for 2h at room temperature. Filter the solution, then wash the resin with a small amount of DCM and mix with the cleavage solution. Pour the resulting solution into 7-10 volumes of cold (0 °C) methyl-tert-butyl ether (MTBE). Allow the suspension to age for 30min at 0 °C, then centrifuge the resulting precipitate and decant the clear solution. Suspend the residue in an equal volume of MTBE and centrifuge and decant the resulting suspension again. After decanting the clear MTBE solution of precipitated peptides, dry in vacuum at 40 °C overnight.

[0023] Synthesis of Preparation 1: SEQ ID NO:2 The synthesis uses Fmoc-Sieber amide resin with a loading of 0.71 mmol / g. The general SPPS procedure is used with the following modifications. [Table 1] [Table 2]

[0024] Preparation 1 Soft Cleavage: Ten identical deprotection reactions are performed in parallel on resin-bound Preparation 1, each at approximately 0.5 mmol scale, using the following protocol: 1) Add 1.55 g (approximately 0.5 mmol) of resin-bound Preparation 1 to a 40 mL fritted reactor. 2) Swell with 3x15 mL DMF (15 min each). 3) Treat with 3x15 mL 20% Pip / DMF (30 min each). 4) Wash with 4x15 mL DMF followed by 4x15 mL DCM. 5) Add 1.5 mL TFA and 28.5 mL DCM to each of five 40 mL reaction vials. 6) Add one-fifth of Preparation 1 resin-bound (2.75 g) to each TFA solution vial, cap the vial, and mix on a rotary wheel for 5 minutes. 7) Filter the mixture and wash with 100 mL of DCM to bring the total volume of the filtrate to 500 mL. 8) Combine the filtrates and transfer to a round-bottom flask containing 1000 mL of MTBE. 9) Concentrate the resulting suspension to a pale yellow oil, triturate with 200 mL of MTBE, and chill in an ice bath for 30 min. 10) Filter the solid, wash with 50 mL of cold MTBE, and dry overnight in a vacuum oven at 33 °C to give 5.35 g (91% yield) of a white solid. Analysis of the isolated solid using UPLC (98.57 area %, combined t-Bu deprotection by-product 0.99%).

[0025] Synthesis of preparation 2: SEQ ID NO:3 The synthesis uses Fmoc-Gly-OH2-CTC resin with a loading of 0.61 mmol / g. The general SPPS procedure is used with the following modifications. [Table 3] [Table 4]

[0026] Preparation 2 Soft Cleavage: To a 40 mL glass scintillation vial, add resin-bound Preparation 2 (3.06 g, 1.12 mmol) and 30 mL of 30% HFIP DCM solution; observe the solution turn red. Rotate the vial at ambient temperature on a rotary wheel for 1 h and agitate. Filter off the resin and wash with 3x10 mL DCM. Remove the solvent under vacuum to form a glassy foam (35 °C bath, 10 torr, 2.34 g) and replace with a small amount of IPA (24 mL) before adding water (24 mL) dropwise at room temperature over 25 min. Stir the resulting solution for 30 min and then filter. Remove with 3x10 mL of H 2 The O cake is washed and then dried overnight in a vacuum oven at 25 torr and 35° C. This produces Preparation 2 as a white solid (1.81 g).

[0027] Synthesis of preparation 4: SEQ ID NO:4 The synthesis uses Fmoc-Leu-OH2-CTC resin with a loading of 0.68 mmol / g. The general SPPS procedure is used with the following modifications. [Table 5] [Table 6]

[0028] Preparation 4 Soft Cleavage: To a 20 mL glass scintillation vial, add Preparation 4 bound to resin (2.0 g, 0.62 mmol) and 10 mL of 30% HFIP DCM solution; observe that the solution turns red. Rotate the vial on a rotary wheel at ambient temperature to stir, then filter off the resin, wash with 3x2 mL DCM, and remove the solvent under vacuum to form a glassy, ​​sticky foam. Dissolve the foam in 5.2 mL DMSO. Add 6 mL of water to this solution at equal flow rates (temperature approximately 15 °C) over 45 min, then add 1 mL of water. Once the peptide solution has been completely added, add another 6 mL of water over 45 min. A white solid precipitates upon addition. Stir the resulting slurry at 15 °C for 30 min. Filter the solid, wash with 6 mL of water, then transfer to a 35 °C, 25 torr vacuum oven. This gives Preparation 4 (Boc-1-14-OH, 1.0763 g) as a white fluffy solid.

[0029] Synthesis of preparation 3 by LPPS: SEQ ID NO:5 A 20 mL glass scintillation vial is charged with Preparation 2 (500 mg, 0.183 mmol), Preparation 1 (179 mg, 0.175 mmol), and DMSO (10 mL). To this solution is added DIEA (46 μL, 0.265 mmol), followed by PyBOP (benzotriazol-1-yloxy)tripyrrolidinophosphonium hexafluorophosphate) (123 mg, 0.230 mmol). The reaction is stirred for 2 hours, then diethylamine (DEA) (183 microliters, 1.77 mmol) is added, and the resulting solution is stirred for 2 hours. The contents of the reaction are drawn into a syringe and added to a stirred 50 mL flask while water (12 mL) is added dropwise over 1 hour. Once addition is complete, the precipitated product is collected by filtration, followed by washing with water (2x4 mL). The wet cake was dried under vacuum at 35° C. for 18 hours to give Preparation 3 as a white solid (0.6003 g, 88% yield, C 184 H 261 N 31 O 38HRMS calculated predicted value: 3512.9444, actual value: 3512.9430).

[0030] Synthesis of preparation 5 via LPPS: SEQ ID NO:6 [ka]

[0031] A 20 mL glass scintillation vial is charged with Preparation 3 (338.8 mg, 0.091 mmol), Preparation 4 (192.1 mg, 0.091 mmol) and DMSO (10 mL). To this solution is added PyBOP (63.5 mg, 0.118 mmol) followed by DIEA (79 microliters, 0.454 mmol). The reaction is stirred for 2.5 hours. The contents of the reaction are drawn into a syringe and added to a stirred 50 mL flask while water (12 mL) is added dropwise over 1 hour. Once the addition is complete, the precipitated product is collected by filtration followed by washing with water (2x4 mL). The wet cake is dried under vacuum at 35°C for 18 hours to give Preparation 5 as a white solid (0.3568 g, 70% yield, C 293 H 435 N 45 O 64 HRMS calculated predicted value: 5608.2168, actual value: 5608.2066).

[0032] Synthesis of Preparation 6 by Method 1 (LPPS) [ka] [ka]

[0033] Eicosanedioic acid, mono(1,1-dimethylethyl) ester (15.0 kg, limiting reactant) and N-hydroxy-succinimide (1.2 equiv.) are dissolved in ethyl acetate at 27 °C. A solution of DCC (1.25 equiv.) dissolved in ethyl acetate is added and the reaction is stirred at 22 °C for 24 h. The resulting DCU by-product is filtered off and the organic phase is extracted three times with 5% aqueous NaCl solution. After extraction, the organic phase is concentrated, coevaporated with isopropanol and crystallized by adding heptane. After filtration, the filter cake is rinsed with heptane and dried at 25 °C to obtain 17.0 kg of INT1 in 87% yield and 99% purity.

[0034] H-Glu-OtBu (7.7 kg, 1.1 equiv.) is dissolved in DCM (54 L) at 20° C., then a solution of TMSA (11.3 kg) dissolved in DCM (7 L) is added and the reaction mixture is stirred at 40° C. for 1 h. INT1 (17.0 kg) in DCM solution is added at room temperature and stirred for 8 h. After the reaction is complete, DCM is exchanged for ethyl acetate by distillation. The organic phase is washed three times with 2% aqueous KHSO 4 . Then it is diluted with 2% aqueous NaCl. 4 The organic phase is concentrated with isopropanol, diluted with isopropanol and crystallized by adding water. After filtration, the filter cake is washed with a water / isopropanol mixture and dried at 30° C. to produce 17.3 kg of INT2 in 86% yield and 99% purity.

[0035] INT2 (17.3 kg) and N-hydroxy-succinimide (4.1 kg, 1.2 equiv.) are dissolved in ethyl acetate (336 kg) at 27 °C. A solution of DCC (8.33 kg, 1.25 equiv.) in ethyl acetate is added and the reaction is stirred at 22 °C for 24 h. The resulting DCU by-product is filtered off. The organic phase is concentrated and coevaporated with isopropanol, then crystallized by cooling the isopropanol solution (approximately 125 L). The filter cake is then rinsed with cold isopropanol and dried at 25 °C to give 16.3 kg of INT3 in 81% yield and 96% purity.

[0036] 17-Amino-10-oxo-3,6,12,15-tetraoxa-9-azaheptadecanoic acid (AEEA2) (8.1 kg, 26.3 mol) is suspended in DCM (54 L) at 22 °C, TMSA (7.68 kg, 59.9 mol) is dissolved in DCM (6.2 L) and the reaction mixture is stirred at 40 °C for 1 h. INT3 (16 kg) is suspended in DCM (31 L) at 35 °C and added to the TMS protected (AEEA2) mixture at 22 °C. The reaction is stirred for 12 h and after completion of the reaction, the mixture is concentrated and then exchanged into ethyl acetate. The organic phase is washed three times with 2% aqueous KHSO 4 Wash 4 times with 2% aqueous NaCl (about 200 L) and then 2% aqueous NaCl (about 200 L) to a target pH of 4.5. Concentrate the organic phase and exchange into acetonitrile. Cool the acetonitrile solution to -20°C and age the resulting suspension at -20°C for 15 hours. Filter the mixture and rinse the filter cake with cold acetonitrile and dry below 0°C to give 18.4 kg of Preparation 6 (88% yield) with 96% purity. Overall yield=53%.

[0037] Synthesis of Preparation 6 by Method 2 (SPPS) Alternatively, preparation 6 can be prepared using solid phase peptide synthesis using a peptide synthesizer.

[0038] Standard coupling procedures are utilized.

[0039] Standard coupling conditions: Deprotection with 0.133M, 2.0 eq. HATU, 5.0 eq. DIEA, ambient temperature, 3 h, 20% piperidine / DMF 3x15 min.

[0040] Resin filling: FmocNH-AEEA on 2-CTC resin (0.99 mmol / g): 1.01 g for each parallel reaction.

[0041] An automated program using a DMF swell followed by Pip / DMF; DMF wash; amino acid, DIEA, HATU mix; and a DMF wash cycle followed by drying.

[0042] The resin is cleaved by stirring the combined lots with 30% HFIP / DCM (240 mL) for 1.5 hours. The resin is filtered, washed, and the solvent is removed from the filtrate under vacuum. The resulting oil is dissolved in acetonitrile, and the solvent is again removed. This procedure gives 30.47 g (146% of theoretical yield) of a viscous yellow oil containing 52.3 area % of the desired product by UPLC analysis. The crude product is purified by flash chromatography (500 grams of silica gel, eluting with 85% DCM / 10% methanol / 5% acetic acid, collecting 38 x 100 mL fractions). The previously chromatographed concentrate (17.94 g) is crystallized to give 13.4 g (74.7% yield) with a UPLC purity of 91.65 area %.

[0043] Example 1 [ka] [ka]

[0044] Synthesis Example 1 SEQ ID NO:1 A first HPLC vial is charged with Preparation 5 (10.5 mg, 0.00187 mmol) and DCM (200 μL, 20 L / kg). To this solution is added a solution of phenylsilane (0.81 M in DCM, 22.1 μL, 0.0178 mmol) and tetrakis(triphenylphosphine)-palladium(0) (0.8 M in DCM, 22.1 μL, 0.00064 mmol). The solution is stirred at 24° C. for 1 hour to obtain a non-isolated solution of Preparation 7 (SEQ ID NO: 7). To a second HPLC vial, add DCM (150 μL), followed by Preparation 6 (0.118 M in DCM, 16 μL, 0.00189 mmol), PyBOP (0.186 M in DCM, 16 μL, 0.00298 mmol) and DIEA (0.573 M in DCM, 5 eq.). The contents of the second vial are added to the first vial and the reaction is stirred for 1 hour to give an unisolated solution of Preparation 8 (SEQ ID NO: 8). The solution of Preparation 8 is concentrated under vacuum and to the resulting solid is added 50 μL of a solution of trifluoroacetic acid (4.65 mL), triisopropylsilane (20 μL) and DTT (20 mg). The slurry is stirred for 18 hours and monitored by HPLC to confirm the formation of Example 1 (C 225 H 348 N 48 O 68 HRMS calculated predicted value: 4810.5249, actual value: 4810.5257).

[0045] Synthesis of Preparation 9 SEQ ID NO:9 Sieber amide resin (13.42 g, 0.75 mmol / g, 10.1 mmol) is suspended in DMF (130 mL, 10 vol) for approximately 20 min, then drained. The resulting resin is washed with DMF (80 mL, 6 vol) for approximately 5 min. The Fmoc amino acid resin is treated with 5 vol% piperidine, 1.25 vol% DBU, and 1.0 wt% HOBt / DMF solution (80 mL, 6 vol) twice for 10 and 20 min, respectively, to remove the Fmoc group. After draining the Fmoc removal solution, it is washed twice with DMF (80 mL, 6 vol), twice with MTBE (80 mL, 6 vol), and again twice with DMF (80 mL, 6 vol).

[0046] Standard Fmoc chemistry is used to carry out amino acid chain assembly. Typically, 1.5 equivalents of Fmoc-amino acid and HOBt (2.47 g, 20% wet, 14.6 mmol, 1.46 equiv) are dissolved in DMF (60 mL, 4.5 vol), followed by the addition of DIEA (1.94 mL, 11.1 mmol, 1.11 equiv). The resulting solution is cooled to below 5 °C in an ice bath and activated by the addition of TBTU (4.83 g, 15.0 mmol, 1.5 equiv). Allow to stand at 0 °C–5 °C for approximately 5 min. DCM (60 mL, 1.5 vol) is added to the resin, followed by the activated Fmoc-amino acid solution. The resulting mixture is stirred at approximately ambient temperature for 2 h. The de-Fmoc procedure is repeated, coupling with the remaining amino acids in sequence. Once the final Fmoc deprotection step is complete, wash the resin twice for 5 min with 2-propanol (130 mL, 10 vol), followed by six washes with MTBE (130 mL, 10 vol). Dry the resin in vacuo at 35 °C to give preparation 9-Seiber (21.21 g, 0.435 mmol / g theoretical, 91.7% yield based on mass gain).

[0047] A portion of Preparation 9 resin complex (10.15 g, 0.435 mmol / g, 4.41 mmol) is treated with a 5 vol% TFA in DCM (101 mL, 10 vol) solution and a DCM wash step. The cleavage fraction and washes are neutralized with DIEA (26.29 g, 35.5 mL, 1.01:1 molar ratio to TFA). The fractions are combined and concentrated under vacuum to 50% of the original volume. Saturated NaHCO 3 Wash the DCM solution with water (2 x 94 mL). 4 The mixture is dried over low heat and concentrated to dryness until a gummy solid is obtained. The gummy solid is reslurried in MTBE (100 mL) at <5°C to break down the gum and give a white slurry product. The white powder slurry from Preparation 9 is filtered, washed, and dried to give a white powder (3.84 g, 92.3 area %, 37.8 wt % DIEA TFA, 57.4 wt %, 2.29 mmol, 51.9% yield, C 46 H 78 N 10 O 12HRMS calculated predicted value: 962.5801, actual value: 962.5806).

[0048] Synthesis of Preparation 10 SEQ ID NO:10 The Fmoc-Gly-Gly-O-2CTC resin complex (18.09 g, 0.57 mmol / g, 10.3 mmol) is suspended in DMF (180 mL, 10 vol) for 20 min and then drained. The resulting resin is washed with DMF (108 mL, 6 vol) for 5 min. The Fmoc amino acid resin is treated twice with 5 vol% piperidine, 1.25 vol% DBU, and 1.0 wt% HOBt / DMF solution (108 mL, 6 vol) for 10 and 20 min, respectively, to remove the Fmoc groups. The de-Fmoc solution is drained and the resin is washed twice with DMF (110 mL, 6 vol), twice with MTBE (110 mL, 6 vol), and twice with DMF (110 mL, 6 vol). Chain assembly is performed by standard Fmoc chemistry.

[0049] For the coupling of amino acids, generally 1.5 equivalents of Fmoc-amino acid and HOBt (2.54 g, 20% wet, 15.0 mmol, 1.5 equiv.) are dissolved in DMF (80 mL, 4.4 vol), followed by the addition of DIEA (1.94 g, 15.0 mmol, 1.5 equiv.) to result in the coupling of amino acids. The resulting solution is cooled to 0-5 °C in an ice bath and activated by the addition of 2-(1H-benzotriazol-1-yl)-1,1,3,3-tetramethylaminium tetrafluoroborate (TBTU) (4.84 g, 15.1 mmol, 1.5 equiv.). Allow to stand at 0-5 °C for 5 min. Then, DCM (35 g, 1.5 vol.) is added to the resin, followed by the addition of the activated Fmoc-amino acid solution. The resulting mixture is stirred at room temperature for 2 h. After completion of the synthesis steps, wash the peptide-resin twice for 5 min with 2-propanol (180 mL, 10 vol), then with MTBE (180 mL, 10 vol each, 6 times) before drying at 35 °C to obtain the prepared 10-resin complex (25.52 g, 0.216 mmol / g, 53.6% yield).

[0050] A portion of the preparation 10 resin complex (10.075 g, 0.216 mmol / g, 2.18 mmol) is treated three times with 1 vol% TFA in DCM (100 mL, 10 vol) and washed with DCM (75 mL, 7.5 vol). The cleavage fraction is neutralized and washed with pyridine (3.18 g, 1.01:1 molar ratio with respect to TFA). The fractions are combined and concentrated under vacuum and dried below 35 °C. Reconstitution is carried out in ethanol (40 mL, 10% vol of the combined filtrate) followed by concentration to dryness. Finally, the peptide is triturated in deionized water (150 mL, 40% vol of the combined filtrate) with stirring. The solid crude peptide precipitate is collected by centrifugation and washed twice with deionized water (150 mL each). The solid is washed twice with n-heptane (100 mL each), isolated, and dried under vacuum at 40 °C to give Preparation 10 (SEQ ID NO:10) as a crisp, pale yellow solid (4.10 g, 72.4 area %, 3.0 wt % pyridine·TFA, 70.2 wt %, 1.85 mmol, 85.1% yield, C 88 H 103 N 11 O 15 HRMS calculated predicted value: 1553.7635, actual value: 1553.7656).

[0051] Synthesis of Preparation 11 SEQ ID NO:11 H-Alanine-O-2CTC resin complex (40.39 g, 0.5 mmol / g, 20.20 mmol) is suspended in DMF (400 mL, 10 vol) for approximately 20 min and then allowed to drain. The resulting resin is washed twice for 5 min with DMF (400 mL, 10 vol). Standard Fmoc chemistry is used to perform amino acid chain assembly. Generally, 1.5 equivalents of Fmoc-amino acid and HOBt (5.51 g, 80 wt%, 32.6 mmol, 1.6 equiv) are dissolved in DMF (150 mL, 3.7 vol), followed by the addition of DIEA (4.22 g, 32.7 mmol, 1.6 equiv). The resulting solution is cooled in an ice bath to approximately below 5 °C and activated by the addition of TBTU (10.39 g, 32.4 mmol, 1.6 equiv). Stir at 0-5 °C for approximately 5 min. DCM (80 mL, 2 vol) is added to the resin followed by the activated Fmoc-amino acid solution, and the resulting mixture is stirred at about ambient temperature for 2 hours.

[0052] The Fmoc amino acid resin is treated with 5 vol% piperidine, 1.25 vol% DBU, 1.0 wt% HOBt / DMF solution (240 mL, 6 vol) twice for 10 and 20 min, respectively, to remove the Fmoc group. The Fmoc-removal solution is drained and the resin is washed twice with DMF (240 mL, 6 vol), twice with MTBE (240 mL, 6 vol), and twice with DMF (240 mL, 6 vol). After completion of the synthesis steps, the peptide resin is thoroughly washed twice with 2-propanol (400 mL, 10 vol) and MTBE (6 times each with 400 mL, 10 vol), then dried under vacuum at 35 °C to obtain the loaded resin minus the last amino acid (74.82 g, 0.159 mmol / g, 11.90 mmol, 58.9% yield). The last amino acid, Fmoc-Leu-OH, is added separately to a portion of the resin (13.61 g, 0.159 mmol / g, 2.16 mmol). The resin is swelled in DMF (130 mL, 10 vol, 3 times) for >5 min each, then deprotected for 10 and 20 min (2 times 130 mL, 10 vol deprotection mixture prepared by dissolving 5.6 g piperidine, 1.67 g DBU, 1.3 g HOBt in 120 mL DMF). The resin is washed with DMF (80 mL, 6 vol, 2 times), MTBE (80 mL, 6 vol, 2 times), and DMF (80 mL, 6 vol, 2 times) for 5 min each. Dissolve in DMF (50 mL, 3.7 vol) followed by the addition of DIEA (0.54 g, 4.2 mmol, 1.9 equiv for coupling of Fmoc-Leu-OH, Fmoc-Leu-OH (1.47 g, 4.16 mmol, 1.9 equiv) and HOBt (0.704 g, 80 wt%, 4.17 mmol, 1.9 equiv) for coupling. Cool the resulting solution to below 5 °C in an ice bath and activate by adding TBTU (1.34 g, 4.17 mmol, 1.9 equiv) and stir at 0-5 °C for 5 min. Add DCM (20 mL, 1.5 vol) to the resin followed by the activated Fmoc-amino acid solution. Stir the resulting mixture at approximately ambient temperature for 2 h. The resin is washed with DMF (180 mL, 13 vol, 2 times), MTBE (180 mL, 13 vol, 2 times), and DMF (180 mL, 13 vol, 2 times) for 5 min each.The resin is washed with DCM (130 mL, 10 vol, 6 times, 5 min each) and then the resin is dried under vacuum at 35° C. to give the loaded resin (12.90 g, 0.203 mmol / g, 2.62 mmol, 121% yield).

[0053] A portion of the resin (7.09 g, 0.203 mmol / g, 1.44 mmol) is treated three times with 1 vol% TFA in DCM solution (70 mL, 10 vol) for 10 min each at approximately ambient temperature, followed by washing with DCM (55 mL, 7.5 vol). The cleavage fraction is neutralized and washed with pyridine (3.02 g, 1.02:1 molar ratio with respect to TFA). The fractions are combined and concentrated under vacuum and dried below 35 °C. Reconstitution is carried out in ethanol (28 mL, 11% vol of the combined filtrate) followed by concentration to dryness. Finally, the peptide is stirred in deionized water (105 mL, 40% vol of the combined filtrate). The solid crude peptide precipitate is collected by filtration and washed with deionized water (4x50 mL). The solid is washed with n-heptane (3x100mL), isolated and dried under vacuum at 40 °C to give Preparation 11 as a white powder (4.54g, 87.6 area%, 44.4wt% pyridine·TFA, 48.7wt%, 0.936mmol, 65.0% yield, C 127 H 192 N 14 O 28 HRMS calculated predicted value 2361.4031, found value 2361.4021). The overall yield of preparation 11 on resin is 71.3%.

[0054] Synthesis of Preparation 12 SEQ ID NO:12 Fmoc-Aib-O-CTC resin complex (19.16 g, 0.54 mmol / g, 10.35 mmol) is suspended in DMF (190 mL, 10 vol) for 20 min and then drained. The resulting resin is washed with DMF (190 mL, 10 vol) for 5 min and then drained. Piperidine (77.82 g), DBU (23.16 g), HOBt (18.09 g, 80 wt%), and DMF (1800 mL) are mixed to give a solution of 5% piperidine, 1.25% DBU, 1.0% HOBt / DMF as the deprotection solution. The Fmoc-amino acid resin is treated with the deprotection solution (190 mL, 10 vol) twice for 10 min and 20 min, respectively, to remove the Fmoc group. Drain the Fmoc removal solution and wash the resin twice with DMF, twice with MTBE, and twice with DMF (190 mL, 10 vol each wash).

[0055] Add DIEA (2.62 g, 20.3 mmol, 2.0 equiv) to a solution of Fmoc-Ile-OH (7.11 g, 10.1 mmol, 2.0 equiv) in DMF (85 mL). Cool the resulting solution to 0-5 °C and add 6-chloro-benzotriazol-1-yloxy-tris-pyrrolidinophosphonium hexafluorophosphate (PyClock) (11.36 g, 20.06 mmol, 2.0 equiv) until completely dissolved. After standing for 3-5 min, add the activation solution to the H-Aib-O-CTC resin complex pre-swollen with DCM (30 mL, 1.5 vol). Allow the reaction to warm to ambient temperature and stir for 2 h. Assay evaluation shows that the unreacted material is approximately 18%. Wash twice with DMF, twice with MTBE, and twice with DMF (190 mL, 10 vol each). A solution of Fmoc-Ile-OH (10.63 g, 30.08 mmol, 6 equiv) in DMF (165 mL) is added to Oxyma (50 mL, 0.6 M in DMF, 30 mmol, 6 equiv) and DIC (50 mL, 0.66 M in DMF, 33 mmol, 6.6 equiv). Stir at about ambient temperature for 5 minutes, then add to the resin and stir for 18 hours. A mixture of pyridine, acetic anhydride, and DMF is added to the resin and stirred for 0.5 hours. The resin is washed with DMF (5x140 mL, 7 vol), DMF (2x180 mL, 9 vol), MTBE (2x180 mL, 9 vol), then DMF (2x180 mL, 9 vol).

[0056] The remaining parts of the chain assembly are carried out in sequence using standard Fmoc chemistry for the remaining amino acids. Generally, Fmoc-amino acid (2.0 equiv.), HOBt (3.42 g, 80 wt%, 2.0 equiv.) are dissolved in DMF (85 mL), followed by the addition of DIEA (2.64 g, 2.0 equiv.). The resulting solution is cooled to 0-5 °C in an ice bath and activated by the addition of TBTU (6.45 g, 2.0 equiv.) and left at 0-5 °C for 3-5 min. DCM (30 mL) is added to the resin, followed by the addition of the activated Fmoc-amino acid solution. The resulting mixture is stirred at room temperature for 2 h. The resulting resin is washed twice with DMF, twice with MTBE, and twice with DMF (190 mL, 10 vol for each wash). The Fmoc-amino acid resin is treated twice with deprotection solution (190 mL, 10 vol) for 10 min and 20 min, respectively, to remove the Fmoc groups. After draining the Fmoc removal solution, the resin is washed twice with DMF, twice with MTBE, and twice with DMF (190 mL, 10 vol each wash).

[0057] Activate the tetramer Boc-Y-Aib-E(tBu)G-OH (12.25 g, 2.0 equiv.) in DMF (50 mL) with Oxyma (30 mL of 0.6 M in DMF, 20 mmol, 2 equiv.) and DIC (33 mL of 0.66 M, 22 mmol, 2.1 equiv.) for 5 min before adding the last four amino acids as a tetramer. Add this mixture to the resin and allow coupling for 18 h. After 18 h, drain the mixture and wash the resin with DMF (5 times, 190 mL, 5 min each). Add the tetramer (6.21 g, 1.0 equiv.) in DMF (40 mL) and activate with PyBOP (5.77 g, 1.1 equiv.) and DIEA (3.32 g, 2.6 equiv.) for 5 min before adding this mixture to the resin and stirring for 4 h. After 4 hours, the mixture is drained and washed with DMF (5 times, 190 mL each, 5 min). The resin is capped by adding a mixture of DMF (105 mL), pyridine (13.48 g, 17 eq.), and acetic anhydride (14.27 g, 14 eq.) and stirred for 1 hour. After chain assembly is complete, the peptide-resin is washed 5 times (190 mL each) with DMF and 6 times (190 mL each) with DCM for 5 min each, then dried under vacuum at 35° C. to give Preparation 12-resin complex (31.03 g, 0.2595 g / mmol theoretical, 8.05 mmol, 77.8% yield). A portion of the preparation 12 resin complex (15.975 g, 0.2595 mmol / g, 4.146 mmol) is treated three times with 1 vol% TFA in DCM solution (160 mL, 10 vol) for 10 min each at ambient temperature, followed by washing with DCM (120 mL, 7.5 vol). The cleavage fraction is neutralized and washed with pyridine (4.74 g, 0.94:1 molar ratio with respect to TFA). The fractions are combined and concentrated under vacuum and dried below 35 °C. Reconstitution is carried out in ethanol (30 mL, 5% vol of the combined filtrate) followed by concentration to dryness. The peptide is mechanically stirred with deionized water (242 mL, 40% vol of the combined filtrate) for 10 min. The solid crude peptide is collected by filtration and washed with deionized water (4x100 mL). The solid is washed with n-heptane (4x100mL), isolated, and dried under vacuum at 35 °C to give Preparation 12 as a white powder (9.38g, 82.2 area%, 0.2wt% pyridine·TFA, 82.1wt%, 3.85mmol, 92.8% yield, C 103 H165 N 13 O 26 HRMS calculated predicted value: 2000.1989, actual measured value: 2000.1968).

[0058] Synthesis of Preparation 13 SEQ ID NO:13 N 2 Add Preparation 9 (2.887 g, 70.2 wt%, 1.30 mmol), Preparation 10 (3.576 g, 57.4 wt%, 2.13 mmol, 1.63 equiv), DMSO (18.1 g, 16.4 mL), DMF (15.8 g, 16.7 mL), and DIEA (655 mg, 5.07 mmol, 3.89 equiv) to the lower flask and stir until a golden yellow solution is obtained. Cool the solution in ice water before adding PyBOP (1.414 g, 2.72 mmol, 2.08 equiv). Remove the ice bath and allow the mixture to warm to ambient temperature. Monitor the reaction for approximately 5 hours to ensure adequate conversion. Add an aliquot of diethylamine (2.116 g, 28.9 mmol, 22.2 equiv) to the reaction mixture at ambient temperature. The mixture is stirred for about 1 hour, resulting in greater than about 99% conversion to Preparation 13. 3 The product is precipitated by adding a mixture containing water (50 mL) and deionized water (50 mL) to the reaction mixture at <4 °C. The mixture is stirred under cold conditions for at least about 15 min. The muddy white slurry is filtered. The wet cake is washed with deionized water (3 × 50 mL) followed by MTBE (6 × 50 mL) and then N for about 62 h. 2 Dry under vacuum with purging at 40° C. This process gave Preparation 13 (4.45 g, 60.4 area %, 16.4 area % dibenzofulvene, 1.18 mmol, 90.5% yield, C 119 H 169 N 21 O 24 HRMS calculated predicted value 2276.2649, found value 2276.2550) is obtained as a pale yellow solid.

[0059] Synthesis of Preparation 14 SEQ ID NO:14 An aliquot of Preparation 11 (3.012 g, 48.7 wt%, 0.621 mmol, 1.00 equiv.) was added to Preparation 13 (3.951 g, 60.4 wt%, 1.05 mmol, 1.69 equiv.), DMSO (9.8 g, 8.9 mL), DMF (52.0 g, 55.0 mL), and DIEA (372 mg, 2.88 mmol, 4.63 equiv.) in a 10 mL flask with N 2 Add to the lower flask. Stir the mixture until a golden solution is obtained. The ice water cools the mixture to less than 10° C. Add an aliquot of PyBOP (742 mg, 1.42 mmol, 2.30 equiv.) to the mixture. Remove the ice bath and allow the mixture to warm to about ambient temperature. Monitor the reaction for conversion to Preparation 14 for about 22 hours. This results in greater than about 96% conversion. When the temperature is less than 10° C., add piperidine (530 mg, 6.22 mmol, 10.0 equiv.) to the cooled reaction mixture. Stir the mixture at ambient temperature for about 2 hours to result in greater than about 99% conversion to Preparation 14. Add the reaction mixture to another flask containing 0.5 N aqueous HCl (12.72 g, 6.23 mmol, 10.0 equiv.) at less than 4° C. and deionized water (16.71 g) to result in precipitation of Preparation 14. Stir the cold slurry for approximately 15 minutes and filter the white slurry. Wash the wet cake with deionized water (2x30 mL), saturated NaHCO 3 Wash with aqueous solution (2x30 mL), deionized water (3x30 mL), MTBE (4x45 mL), then N for approximately 17 h. 2 Dry under vacuum with purging at 40° C. Obtain the product, Preparation 14, as a white powder (5.418 g, 48.9 area %, 0.603 mmol, 97.0% yield, C 231 H 349 N 35 O 49 HRMS calculated predicted value: 4397.5893, actual value: 4397.6057).

[0060] Synthesis of Preparation 15 SEQ ID NO:15 An aliquot of Preparation 12 (671 mg, 82.1 wt%, 0.275 mmol, 1.23 equiv.) was diluted with N 2Add Preparation 14 (2.009 g, 48.9 area%, 10.7 area% isomer, 0.223 mmol, 1.00 equiv), DMSO (11.1 g, 10.0 mL), DMF (19.0 g, 20.1 mL), and DIEA (76 mg, 0.588 mmol, 2.63 equiv) to the flask with stirring to give a golden yellow solution. Add an aliquot of 0.6 M HOAt (619 mg, 0.384 mmol, 1.72 equiv) before cooling to -5 °C. Add a sample of PyClock (220 mg, 0.397 mmol, 1.78 equiv). Allow the mixture to warm to near ambient temperature, resulting in approximately 84% conversion to Preparation 15. Isolate the product by adding the reaction mixture to ice-cold deionized water (548 mL) over 10 min to precipitate the product. Rinse the reaction flask with DMF (5 mL) and add to the slurry. Stir the slurry for approximately 15 minutes, warm to near ambient temperature, and filter. Wash the wet cake with deionized water (3x80 mL) and dry the white waxy solid under vacuum at 35 °C for 3.5 days to give Preparation 15 as a white powder (2.506 g, 41.6 area %, 0.163 mmol, 73.1% yield, C 334 H 512 N 48 O 74 HRMS calculated predicted value: 6379.7777, actual value: 6379.8652).

[0061] Example 2 Synthesis of Example 2 SEQ ID NO:1 A sample of TFA (19.656 g, 13.03 mL) was diluted with DCM (815 mg, 0.62 mL), DTT (434 mg), and TIPS (362 mg, 0.47 mL) and diluted with N 2The mixture is added to the flask under reduced pressure. The mixture is cooled in ice water before adding water (468 mg, 0.47 mL). A sample of Preparation 15 (1016 mg, 39.0 area %, 0.0620 mmol) is added to this mixture at 2° C. to result in a solution. The mixture is allowed to warm to about ambient temperature and stirred for about 2 hours. The reaction mixture is added to MTBE (150 mL) at −15° C. and the reactor is rinsed with MTBE (3 mL). After about 10 minutes the slurry is centrifuged and the supernatant is decanted. The wet cake is reslurried in MTBE (3×50 mL), centrifuged after each wash and the supernatant is decanted. The wet cake is dried under vacuum at 35° C. to give Example 2 as a white solid (784 mg, 26.5 area %, 0.0432 mmol, 69.7% yield, C 225 H 348 N 48 O 68 HRMS calculated predicted value: 4810.5249, actual value: 4810.5642).

[0062] Synthesis of Preparation 16 SEQ ID NO:16 The synthesis uses Fmoc-Gly-OH2-chlorotrityl resin with a loading of 0.61 mmol / g. The general SPPS procedure is essentially as described herein. Preparation 16 results from soft cleavage of the peptide on the resin described herein using methods known to those skilled in the art. Reconstitution of the concentrated material is performed with ethanol (5% vol of the combined filtrates) and concentration to dryness. The peptide is triturated in water with stirring (40% vol of the combined filtrates). The solid is isolated and dried under vacuum at 40° C. to constant weight to give 5.24 g (99%) of Preparation 16 as a white powder.

[0063] Synthesis of Preparation 18 SEQ ID NO:17 The synthesis uses Fmoc-Ala-OH2-chlorotrityl resin with a loading of 0.50 mmol / g. The general SPPS procedure is used essentially as described herein with the following modifications. [Table 7]

[0064] Preparation 18 Soft cutting: A 42.13 g sample of the peptide on resin intermediate is placed in a flask and treated three times with 10 volumes (400 mL) of 1% TFA / DCM for 10 min each, followed by washing with DCM. Each treatment is quenched by adding 4.4 mL of pyridine. The resulting solutions are combined and concentrated under vacuum. Reconstitution is performed in ethanol (25 mL) followed by concentration to dryness to give 56.6 g of a foamy semi-solid. Ten 400 mL portions of water are added to produce a slurry. The slurry is filtered and washed with water. The solid is isolated and dried to constant weight under vacuum at 40 °C to give 23.3 g of Preparation 18 as a white powder.

[0065] Synthesis of preparation 17 ((52S)-52-(((((9H-fluoren-9-yl)methoxy)carbonyl)amino)-25-(tert-butoxycarbonyl)-2,2-dimethyl-4,23,28,37,46-pentaoxo-3,32,35,41,44-pentaoxa-24,29,38,47-tetraazatripentacontan-53-oic acid) Preparation 6 (80 g, 92 mmol), DIEA (17.53 mL, 101 mmol), TSTU (30.3 g, 101 mmol) and acetonitrile (1 L) are placed in a vessel and stirred at 23 °C for 17 h. The solution is concentrated and the resulting orange residue is redissolved in EtOAC (1.6 L) and then washed with 0.1 M HCl (2 × 1 L). The organic layer is washed with water (2 × 1 L) and then with MgSO 4The mixture is dried over hexane, filtered and concentrated under vacuum to leave an orange oil (83 g). A second batch is performed on the same scale, resulting in a combined total of 123 g of crude oil. The intermediate ester (123 g, 110 g active, 113 mmol) is dissolved in EtOH (700 mL), then Fmoc-lysine (45.9 g, 125 mmol) and DIEA (21.70 mL, 125 mmol) are added and the reaction is stirred for 17 h. After completion of the reaction, EtOH is removed under vacuum to leave an orange oil (201 g). The residue is dissolved in EtOAc (1.1 L) and washed with 0.1 M HCl solution (3 x 400 mL), then NaHCO 3 Wash with aqueous solution (400 mL). Separate the layers then wash the organic layer with saturated aqueous sodium chloride (1x400 mL). Concentrate the organics to give an orange oil (~190 g). Add acetone (400 mL) then filter the resulting suspension to remove inorganics. Concentrate the mixture and purify by normal phase chromatography (1.1 kg silica prepared in 60 / 40 heptane / acetone) eluting with increasingly polar eluents (collect ~3 L fractions). Combine and concentrate fractions with at least 95 HPLC area % to give a dark yellow oil (70 g) of Preparation 17.

[0066] Synthesis of Preparation 19A SEQ ID NO:18 The synthesis uses Fmoc-Leu-OH2-chlorotrityl resin with a loading of 0.65 mmol / g. The general SPPS procedure is used with the following modifications. [Table 8] [Table 9]

[0067] Preparation 19A from pseudoproline can be treated in a similar manner to Preparation 19B for Example 3, as described herein.

[0068] Synthesis of Preparation 19B SEQ ID NO:19 The synthesis uses Fmoc-Leu-OH2-chlorotrityl resin with a loading of 0.65 mmol / g. Preparation 19B is prepared using the SPPS procedure essentially as described herein. [Table 10] [Table 11]

[0069] Preparation 19B Soft Cleavage: Preparation 19B is prepared using soft cleavage of resin-bound 19B substantially as described herein using methods known to those of skill in the art. See, e.g., the method of Preparation 18. The resulting solid is isolated and dried under vacuum at 30-40° C. to constant weight to give 2.94 g of product as a pale yellow powder.

[0070] Synthesis of Preparation 20 SEQ ID NO:20 To a solution of Preparation 1 (4.25 g, 4.166 mmol) and Preparation 16 (5.00 g, 3.340 mmol) in DMSO / DMF (1:1, 200 mL) is added PyBOP (2.60 g, 5.00 mmol) and DIEA (1.75 mL, 10.0 mmol) at ambient temperature. The solution is stirred for 18 h and quenched by adding excess diethylamine (10.0 mL) with water. The quenched solution is stirred for 2 h and then slowly added to a solution of saturated aqueous sodium bicarbonate / water (1:1, 300 mL) at 0 °C. The resulting precipitate is stirred for 10 min and then collected by filtration. The filtrate is washed successively with water (3x150 mL) followed by methyl tert-butyl ether (3x150 mL). Dry the solid under vacuum at 40° C. to give Preparation 20 as a white solid (5.30 g, 69% yield, C 119 H 169 N 21 O 24 HRMS calculated predicted value: 2276.2649, actual value: 2276.2652).

[0071] Synthesis of Preparation 21 SEQ ID NO:21 To a solution of Preparation 20 (1.00 g, 0.44 mmol) and Preparation 18 (0.90 g, 0.40 mmol) in DMSO / DMF (1:1, 20 mL) is added PyBOP (314 mg, 0.30 mmol) and DIEA (0.21 mL, 1.20 mmol) at ambient temperature. The solution is stirred for 18 h and then quenched with piperidine (0.79 mL, 4.00 mmol). The quenched solution is stirred for 2 h and then cooled to 0° C. and quenched with a dilute solution of HCl (50 mL). The resulting slurry is stirred for 10 min and the solid is collected by filtration. The filtrate is washed successively with saturated aqueous sodium bicarbonate (2×50 mL), water (3×50 mL), followed by methyl tert-butyl ether (3×50 mL). Dry the solid under vacuum at 40° C. for 18 hours to give Preparation 21 as a white solid (1.80 g, 106% yield, C 225 H 338 N 34 O 48 HRMS calculated value: 4284.5053, measured value: 4284.5062).

[0072] Synthesis of Preparation 22 SEQ ID NO:22 To a solution of Preparation 21 (214 mg, 0.05 mmol) and Preparation 19B (116 mg, 0.055 mmol) in DMSO / DMF (1:1, 3 mL) is added PyBOP (57 mg, 0.11 mmol) and DIEA (58 μL, 0.33 mmol) at ambient temperature. The solution is stirred for 18 h and then quenched with a 1:1 mixture of saturated aqueous sodium bicarbonate and water (10 mL). The mixture is stirred for 10 min and the resulting solid is collected. Wash the solid with water (3×10 mL) and dry the solid under vacuum at 40° C. to obtain Preparation 22 (285 mg, 89% yield, C 334 H 512 N 48 O 74 HRMS calculated predicted value: 6379.7777, actual value: 6379.7730).

[0073] Example 3 Synthesis of Example 3 SEQ ID NO:1 A solution of TFA (2.3 mL), water (0.1 mL), triisopropylsilane (0.1 mL), and DTT (75 mg) is cooled to 0° C. The solution is charged with Preparation 22 (100 mg, 0.015 mmol) and the reaction mixture is allowed to warm to ambient temperature and stirred for 2 h. The resulting mixture is poured into a pre-cooled (−20° C.) solution of methyl tert-butyl ether (25 mL). The resulting precipitate is kept at −20° C. for 15 min, the slurry is centrifuged, and washed with methyl tert-butyl ether (2×25 mL). The solid is dried under vacuum at 35° C. for 18 h to give Example 3 as a white solid (71 mg, 93% yield, C). 225 H 348 N 46 O 68 HRMS calculated predicted value: 4810.5249, actual value: 4810.5036).

[0074] Step 1 Step 1: A feed solution of preparation 25 (1.05 eq.) is prepared in 5 vol DMSO / ACN (90:10 vol / vol). A second feed solution of preparation 26 is prepared in 20 vol DMSO / ACN (90:10 vol / vol). A third feed solution is prepared from PyOxim (1.5 eq.) in 3 vol ACN. A fourth stream of DIEA in ACN (4 eq.) is prepared. The first three streams are pumped into a mixer, where DIEA is mixed at the mixer outlet, and the mixture is pumped through another mixer and a plug flow reactor to a thermostatic bath at 20° C., where it remains for 2 hours. At the reactor outlet, acetic acid can be added to consume the remaining PyOxim (1-cyano-2-ethoxy-2-oxoethylideneaminooxy-tris-pyrrolidino-phosphonium hexafluorophosphate). After 2 more hours, neat diethylamine (10 equivalents) is added and mixed in the mixer. The flow passes to a second plug flow reactor and is held in a 20°C bath for 1 hour. The product solution of Preparation 27 is collected and sent to nanofiltration using a 70 / 30 DMSO / ACN solution to remove 10-20 diavolumes of reagents.

[0075] A feed solution of Preparation 25 (2.40 kg, 96.7 wt%, 2.274 mol) is prepared by dissolving the solid in DMSO (13.88 kg, 12.62 L) and diluting the solution with ACN (1.09 kg, 1.39 L) to create a solution of Preparation 25 (114.3 mg / mL, 0.112 M) in 90:10 vol / vol DMSO:ACN. A second feed solution of Preparation 26 (SEQ ID NO:26, 2.79 kg, 98.6 wt%, 1.836 mol) is prepared by dissolving the solid in DMSO (54.8 kg, 49.8 L) and diluting the solution with ACN (4.3 kg, 5.47 L) to create a solution of Preparation 26 (45.5 mg / mL, 0.030 M) in 90:10 vol / vol DMSO:ACN. A third feed solution is prepared with PyOxim (4.5 kg, 8.53 mol) in ACN (47.33 kg, 60.22 L) to produce a 0.132 M solution. DIEA is added neat. A stream of solution of Preparation 25 (14.91 L, 1.704 kg, 1.670 mol, 0.95 eq, 5.9 g / min), a stream of Preparation 26 (58.46 L, 2.660 kg, 1.750 mol, 1.00 eq, 22.5 g / min), and a stream of PyOxim (1.4 eq, 5.4 g / min) are mixed with neat DIEA (4.0 eq, 0.446 mL / min) at 20° C. and pumped to the mixer. The mixture is pumped through another mixer and a plug flow reactor to a 20° C. thermostatic bath and after a 3 hour residence time, collection over 42.9 hours results in 88.6 kg of product solution.

[0076] Nanofiltration is a membrane-based filtration process used to separate chemical species based on differences in size and molecular weight. The product solution of preparation 27 contains reagents (diethylamine, PyOxim, DIEA, etc.) and unwanted by-products (e.g., dibenzofulvene) that need to be removed before proceeding to the next step. Nanofiltration is applied to remove undesired species (molecular weight less than 500 Da).

[0077] The Preparation 27 product solution is charged to the NF feed tank and pumped in a recirculation loop through a heat exchanger and a nanofiltration unit containing an appropriate membrane (ceramic or polymer) to cause the desired separation. Undesired species are removed from the permeate and either collected separately or discarded. To maintain a constant volume in the NF tank, fresh solvent, i.e., 70:30 vol / vol DMSO / ACN, is pumped in continuously to match the permeate rate being withdrawn. The Preparation 27 product solution is purified by nanofiltration and conveyed directly to Step 2.

[0078] A solution of Fmoc-protected Preparation 27 in DMSO / ACN (88.6 kg) and diethylamine (1.34 kg) is added to the reactor. The mixture is stirred at 20° C. for 2 h to result in Preparation 27 (87.6 L, 38.45 mg / mL, 3.37 kg, 1.48 mol). The product solution of Preparation 27 is charged to a nanofiltration feed tank and then pumped in a recirculation loop through a heat exchanger and a nanofiltration unit containing an appropriate membrane (ceramic or polymer) to cause the desired separation. Undesired species are removed on the permeate side and collected separately or discarded. This operation is continued until sufficient removal of undesired impurities is achieved. To maintain a constant volume in the nanofiltration tank, fresh 70:30 vol / vol DMSO / ACN is continuously pumped in to match the permeate rate being withdrawn. This gives preparation 27 in DMSO / ACN (72.4 L, 40.8 mg / mL, 2.95 kg, 1.30 mol, 78.1% yield overall for coupling, de-Fmoc, and nanofiltration).

[0079] Step 1 Example - Analysis results. HPLC confirms the conversion of Preparation 25 and Preparation 26 to form Preparation 27. The analytical method uses a (2.1 mm ID x 150 mm x 1.7 micron particle size) phenylhexyl stationary phase column at 65°C with a 2-98% B gradient of 0.1% TFA in water and acetonitrile over 12 minutes. UV detection at 214 nm is used for this material.

[0080] Table A.1 shows the high resolution mass spectrometry data collected on the product of the Step 1 coupling reaction (Fmoc protected preparation 27) and the product of the Step 1 deprotection reaction (preparation 27). Mass accuracy is the metric used to confirm the match between measured and expected species. [Table 12] Table A.1 Confirmation of Fmoc-protected preparation 27 measured and preparation 27 with mass accuracy calculated using high resolution mass spectrometry data.

[0081] Step 2 [ka]

[0082] Scheme A.2 Synthesis of Preparation 29 (SEQ ID NO:29) from Fragment Preparation 27 (SEQ ID NO:27) and Preparation 28 (SEQ ID NO:28). [ka]

[0083] Step 2: A feed solution of preparation 28 (1.15 eq.) is prepared in 10 vol DMSO / ACN (90:10 vol / vol). A second feed solution is prepared with PyOxim (2 eq.) in 1 vol ACN. A third stream of DIEA (3 eq.) in ACN is prepared (5 wt % solution). The stream of preparation 27 solution from step 1, the stream of preparation 28 and the stream of PyOxim are pumped into a mixer and mixed with DIEA at the mixer outlet, the mixture is pumped through another mixer and a plug flow reactor to a thermostatic bath at 20° C., where it dwells for 2 hours. At the reactor outlet, acetic acid can be added to consume the residual PyOxim. After more than 2 hours, neat diethylamine (10 eq.) is added and mixed in the mixer. This stream goes to a second plug flow reactor and dwells for 1 hour in a thermostatic bath at 20° C. Collect the product solution of Preparation 29 and send the DMF solution as the diafiltrate to nanofiltration to remove 10-20 diavolumes of reagent.

[0084] A feed solution of Preparation 28 (4.68 kg, 98.9 wt%, 2.058 mol) is prepared by dissolving the solid in DMSO (41.75 kg, 37.95 L) and diluting the solution with ACN (3.3 kg, 4.20 L) to create a solution of Preparation 28 (94.7 mg / mL, 0.0421 M) in 90:10 vol / vol DMSO:ACN. A second feed solution is prepared with PyOxim (3.0 kg, 5.69 mol) in ACN (11.81 kg, 15.03 L) to produce a 0.327 M solution. DIEA is added neat. A stream of solution of Preparation 27 from step 1 (73.86 L, 41.2 mg / mL, 3.04 kg, 1.336 mol, 0.0181 M, 1.0 eq, 29.9 g / min), a stream of Preparation 28 (1.3 eq, 17.7 g / min) and a stream of PyOxim (2.1 eq, 2.9 g / min) are pumped to a mixer, at the outlet of which the streams are adjusted to 20° C. and mixed with neat DIEA (4.0 eq, 0.374 mL / min) at 20° C. The mixture is pumped through another mixer and a plug flow reactor to a thermostatic bath at 20° C., and after a residence time of 3 hours, collection over 43.2 hours results in 129.35 kg of the product solution of Preparation 29.

[0085] In a nanofiltration process substantially as described above, the product solution of formulation 29 is used in place of the product solution of formulation 27.

[0086] Nanofiltration process using Fmoc-protected preparation 29 solution in DMSO / ACN is carried out substantially as described herein. Fmoc-protected preparation 29 (129.35 kg) and diethylamine (2.0 kg) are charged to a reactor for nanofiltration. Nanofiltration process results in preparation 29 in DMF (98.85 L, 42.24 mg / mL, 4.18 kg, 0.974 mol, 73.1% yield overall for coupling, de-Fmoc, and nanofiltration).

[0087] HPLC confirms the synthesis of Preparation 29 from Preparation 28 and Preparation 27. The analytical method uses a (2.1 mm ID x 150 mm x 1.7 micron particle size) C4 stationary phase column at 65 °C with a 25-98% B gradient of 0.1% TFA in water and acetonitrile over 12 minutes. UV detection at 214 nm is used for this material.

[0088] Table A.3 shows the high resolution mass spectrometry data collected on the product of the Step 2 coupling reaction (Fmoc protected Preparation 29) and the product of the Step 2 deprotection reaction (Preparation 29). The mass accuracy confirms the measured species product, monoisotopic mass of the neutral species. [Table 13] Table A.3 Confirmation of Measured Fmoc-Protected Preparation 29 and Preparation 29 with Calculated Mass Accuracy Using High Resolution Mass Spectrometric Data.

[0089] Step 3 Scheme A.3 Synthesis of Preparation 31 (SEQ ID NO: 31) from Fragment Preparation 30 (SEQ ID NO: 30) and Preparation 29 (SEQ ID NO: 29). [ka]

[0090] Step 3 Batch Process Description: Nanofiltered DMF solutions of Preparation 29 (2.249 g, 46.5 mg / g, 104.6 bmg, 0.0244 mmol) and Preparation 30 (71.5 mg, 90.6 area%, 0.0306 mmol) in DMF (0.3068 g, 0.325 mL) at -5 °C are mixed with a 5.0 wt% solution of DIEA in DMF (114.0 mg, 5.70 mg of DIEA, 0.0441 mmol, 1.8 equiv.) and a 10.1 wt% solution of 1-[bis(dimethylamino)methylene]-1H-1,2,3-triazolo[4,5-b]pyridinium 3-oxide hexafluorophosphine oxide in DMF (1.0 mg, 0.0241 mmol, 0.0241 mmol) in DMF (0.0241 mmol). Add phosphate (HATU) (154.9 mg, 15.59 mg HATU, 0.0410 mmol, 1.7 equiv). Stir the solution at -5°C for 4 hours and then quench with 5 wt% aqueous sodium bicarbonate (5.295 g, 4.8 mL) over 15 minutes at ambient temperature. Stir the resulting slurry at 0°C for 15 minutes and collect the resulting solid by filtration. Wash the solid with water (4x2 mL) and then with MTBE (4x2 mL). Dry the sticky solid under vacuum at 35°C to give Preparation 31 (219.7 mg, 47.6 area%, 0.0164 mmol, 67.1% yield).

[0091] A feed solution of preparation 30 is prepared with 10 volumes of DMF. A second feed solution is prepared with HATU (1.8 equivalents) in a 10 wt% solution with ACN. A third stream of DIEA (2.5 equivalents) in DMF is prepared (5 wt% solution). The stream of solution of preparation 29 from step 2, the stream of preparation 30, and the stream of DIEA are pumped to a mixer, at the outlet of the mixer the streams are cooled and mixed with the cooled HATU solution. The mixture is pumped through another mixer and a plug flow reactor to a thermostatic bath at -5°C, where it is collected after a residence time of 3 hours. A solution of brine / bicarbonate (17 wt% aqueous sodium chloride, 0.5 wt% sodium bicarbonate solution) with a salt load of 19 wt% is prepared. The product solution of preparation 31 in DMF is then pumped with the salt solution to a mixed product mixing suspension reactor (MSMPR) to form a precipitate. The tau of the mixed product mixed suspension reactor is 1 hour. A second MSMPR is performed at low temperature for 1 hour tau and the slurry is intermittently loaded onto the filter. The slurry is washed with water and dried under vacuum at 35°C.

[0092] A feed solution of Preparation 30 (9.42 kg, 83.6 wt%, 3.72 mol) is prepared in DMF (54.12 kg) to make a 0.0563 M feed. A second feed solution is prepared with HATU (1.15 kg, 3.02 mol) in ACN (10.4 kg) to make a 0.215 M feed. DIEA is added neat. A stream of Preparation 29 solution from step 2 (98.85 L, 42.24 mg / mL, 4.18 kg, 0.975 mol, 0.0099 M, 1.0 equiv, 40.2 g / min), a stream of Preparation 30 (1.3 equiv, 9.2 g / min), and a stream of DIEA (2.1 equiv, 0.152 mL / min) are pumped to the mixer. At the mixer outlet, the stream is cooled to 0°C and mixed with HATU solution (2.0 equiv., 3.2 g / min) cooled at 0°C. The mixture is pumped through another mixer and plug flow reactor to a thermostatic bath at 0°C, where it is collected over 42 hours after a 4 hour residence time, resulting in 131.8 kg of product solution. The product solution is precipitated in two sections. 17 wt% NaCl aqueous solution / 0.5 wt% NaHCO 3The aqueous solution (29 kg) is mixed with DMF (13.2 kg) in an inerted reactor and cooled to below 20° C. The product solution in DMF (66.6 kg) is then diluted with 17 wt % aqueous NaCl / 0.5 wt % NaHCO 3 Aqueous solution (34.4 kg) is co-added to the reactor over 1 hour and maintained at 20°C resulting in precipitation of the product, Preparation 31. The slurry is cooled to 5°C over 1 hour and then water is added in two portions (total 32.2 kg). The slurry at 5°C is stirred for 0.5 hours before filtering the slurry. The wet cake is reslurried with water (63.9 kg) for 0.5 hours and filtered. A second section of the product solution is precipitated in an identical manner. 17 wt% aqueous NaCl / 0.5 wt% NaHCO 3 A solution of water (29 kg) and DMF (13.55 kg) is mixed in a reactor and cooled to below 20° C. A second section of the product solution in DMF (65.2 kg) is diluted with 17 wt % NaCl aqueous solution / 0.5 wt % NaHCO 3 The aqueous solution (36.8 kg) is co-added to the reactor over 1 hour and maintained at 20° C. resulting in precipitation of the product, Preparation 31. The slurry is cooled to 5° C. over 1.25 hours before water is added in two portions (32.1 kg total). The slurry is stirred for 0.5 hours and filtered onto the first wet cake. The combined wet cakes are reslurried twice with water (64 kg each) for 0.5 hours each and filtered. This is followed by two displacement washes with water (64 kg each). The combined washed wet cakes are purged with N 2 and then dried under vacuum at 38° C. until the KF is less than 4 wt %, resulting in Preparation 31 (10.34 kg, estimated potency 60%, 0.972 mol, estimated yield 100%).

[0093] Example 3 Tirzepatide (SEQ ID NO: 1) [ka]

[0094] A solution of TFA (2.3 mL), water (0.1 mL), triisopropylsilane (TIPS, 0.1 mL) and dithiothreitol (DTT, 75 mg) is cooled to 0 °C. Preparation 31 (100 mg, 0.015 mmol) is charged to this solution and the reaction mixture is allowed to warm to ambient temperature and stirred for 2 h. The resulting mixture is poured into a pre-cooled (-20 °C) MTBE solution (25 mL). The resulting precipitate is kept at -20 °C for 15 min, the slurry is centrifuged and washed with MTBE (2 x 25 mL). The solid is dried under vacuum at 35 °C for 18 h to give Example 3 as a white solid (71 mg, 93% yield, C 225 H 348 N 46 O 68 HRMS calculated predicted value: 4810.5249, actual value: 4810.5036).

[0095] A 15°C inerting reactor is charged with DCM (27.3 kg, 20.6 L), water (4.1 kg), Preparation 31 (10.34 kg, estimated potency 60%, 0.972 mol), and DTT (3.10 kg). A separate inerting reactor is charged with TFA (154.1 kg, 103.4 L) and TIPS (3.2 kg, 4.2 L). The TFA / TIPS solution is added to the Preparation 31, DCM, water, and DTT slurry within 0.25 hours to form a colorless solution, warm, and hold at 20°C for 3 hours. After 3 hours at 20°C, the reactor is cooled to -10°C. A separate reactor is charged with MTBE (382.4 kg, 516.8 L) and cooled to -20°C. A portion of this cold MTBE (91.8 kg, 124.1 L) is added to the cold reaction solution over 2 hours while maintaining the temperature at -5°C to -18°C. The remaining cold MTBE (294.3 kg, 397.7 L) is added over 1.5 hours while maintaining the temperature at -5°C to -18°C, resulting in precipitation of Example 3. The slurry is adjusted to 0°C and held for >0.5 hours before filtering into three sections. The wet cake is combined and reslurried twice with MTBE (114.7 kg, 155 L) and filtered before a final MTBE displacement wash (114.7 kg, 155 L). The wet cake is dried at 28°C until less than 4.5 wt% MTBE is measured. This gives Example 3 (7.77 kg, 46.8 wt%, 0.755 mol, 77.7% yield).

[0096] Example 4A (Linear SPPS) Tirzepatide (SEQ ID NO: 1) [ka] [ka]

[0097] Fmoc Sieber resin (17 kg, 0.76 mmol / g) is charged to the reactor. The resin is swelled in DMF and stirred for 2 hours, then the resin is filtered to remove the DMF. The resin is then washed a total of two times with DMF. The Fmoc protected resin is then deprotected using a 20% PIP / NMP treatment. Sampling to confirm Fmoc removal is performed after the final PIP / NMP treatment to confirm >99% Fmoc removal by UV analysis (IPC target <1% residual Fmoc). After the final 20% w / w PIP / NMP treatment, the resin bed is washed multiple times with DMF. The peptide backbone is then constructed using the following general conditions for coupling and deprotection of each amino acid: [Table 14]

[0098] Fmoc deprotection: The resin in the peptide reactor is treated with three or four charges of 20% v / v PIP / NMP solution. Each treatment is stirred on the resin for 30 minutes and then filtered to complete the removal of the Fmoc protecting group. After the final 20% v / v PIP / NMP treatment, the resin bed is washed a minimum of six times with DMF using the pre-specified DMF volumetric loadings.

[0099] Amino acid activation: A pre-prepared solution of 12% w / w Oxyma Pure / NMP is charged to the reactor. The selected Fmoc amino acid is then added. The mixture is stirred at 20±5°C until the Fmoc amino acid is completely dissolved. To ensure control of the slightly exothermic activation reaction, the Fmoc-AA / Oxyma Pure / NMP solution is then cooled to 15±3°C prior to activation, and the resulting solution temperature is maintained in the specified range of 20±5°C. The amino acid solution is then activated by DIC addition. The activated ester solution is then stirred for 20-30 minutes before transferring the solution to the reactor containing the peptide on resin intermediate.

[0100] Coupling: Once the pre-activation step is complete, transfer the activated ester solution to the reactor containing the deprotected peptide on resin to initiate the coupling reaction. Stir the peptide coupling reaction at 20±5°C for at least 4 hours. After the required stirring time, sample the resin slurry for coupling completion (IPC). Repeat sampling at specific intervals as necessary until a passing IPC result is obtained. If necessary, perform a re-coupling operation. Once coupling is complete, filter the contents of the peptide reactor solution and wash the peptide on resin intermediate several times with DMF to prepare for the next coupling.

[0101] Coupling of Ile (12) to Aib (13): Coupling of Fmoc-Ile (12) to Aib (13) is accomplished using a symmetric anhydride approach utilizing 6 equivalents of Fmoc-AA, 3 equivalents of DIC. The activation time for this sequence is extended from 40 to 60 min to ensure formation of the activated symmetric anhydride species. Extended coupling stirring times (18 h) are required to achieve reaction completion (<1% uncoupled) as determined by HPLC analysis.

[0102] Lys(20)ivDe Deprotection (Preparation 23): Selective deprotection of the Lys(20)ivDde group of the 39 amino acids fully protected on the resin Boc-Tyr(1)-Ser(39) peptide backbone is performed. Deprotection is achieved using 8% w / w hydrazine hydrate in DMF solution with stirring at ambient temperature for 4 h. The deprotection reaction is monitored by HPLC, aiming for an IPC limit of less than 1% of Lys(ivDde) ​​moieties remaining after deprotection. The resulting peptide fragment (Preparation 23) is washed repeatedly (8 times) with DMF to completely remove residual hydrazine. The fully assembled Preparation 23 fragment is washed 4 times with IPA and dried at 40 °C or lower until the LOD is 1% or lower. Preparation 23 is packaged and stored refrigerated (-20 °C) before coupling with Preparation 6.

[0103] Coupling of Preparation 6 to Preparation 23: The solids of Preparation 6 (1.5 eq.) and PyBOP (1.5 eq.) are charged to a reactor followed by the addition of DMF and the mixture is stirred until dissolution occurs. Collidine is then charged to initiate the formation of the active ester species. The activated ester solution is stirred for 60 minutes before being transferred to the reactor containing the Preparation 23 intermediate. The reaction slurry is stirred at 25° C. for 18 hours. The slurry is sampled for coupling completion (IPC) and, if necessary, sampling is repeated at specific intervals as necessary to achieve a passing IPC result (1% or less of Preparation 23). Once coupling is complete, the contents of the solution are filtered and discarded. The fully assembled Preparation 24 intermediate is washed multiple times with DMF and then IPA. Preparation 24 is dried at 40° C. or less until an LOD of 1% or less is achieved. Preparation 24 is packaged and stored refrigerated (−20° C.) before being cleaved from the resin.

[0104] Resin cleavage and crude separation of Example 4A: Prepare a cleavage cocktail consisting of trifluoroacetic acid (TFA), triisopropylsilane (TIPS), dithioteritol (DTT), DCM and water. Cool the cleavage cocktail to 15±5° C. The reagent charge is shown in the table below. [Table 15]

[0105] Preparation 24 is charged to the reactor, followed by the cleavage cocktail. The reaction is stirred for 3 hours at 23 °C. The mixture is filtered, then the spent resin is washed with DCM. The DCM wash filtrate is combined with the bulk deprotection solution, and the contents are cooled to below -10 °C. The MTBE is cooled to below -13 °C, then cold MTBE is fed into two portions of the cold filtrate. The MTBE feed rate is controlled to maintain the internal temperature of the crude solution below 5 °C. The first MTBE charge constitutes approximately 45% of the total MTBE charge. A soft precipitate forms near the end of the MTBE addition, but it easily redissolves in solution. The precipitate solution is then recooled to an internal temperature of -15 ± 5 °C. The second MTBE addition is fed at a rate approximately 5-10 times the initial MTBE feed rate, and constitutes approximately 55% of the total MTBE charge. The internal temperature of the precipitate slurry is maintained below 0 °C during the addition. The resulting slurry is aged at -8±3° C. for a minimum of 6 hours, then warmed to 0±3° C. and aged an additional 2 hours before isolation.

[0106] The cold crude peptide slurry is filtered and the resulting wet cake is then washed with MTBE. The crude wet cake of Example 4A is then dried until the IPC target LOD value is 1% or less. The crude product of Example 4A is packaged and stored. The crude intermediate is stored refrigerated (-20°C) until purification. Overall, 45.39 kg of crude Example 4A is produced at 45 wt% and 64% HPLC area percent purity. Content yield based on Sieber resin = 47%.

[0107] Example 4A Purification: Mobile phase: Mobile phase A (MPA) 90% water, 0.1% TFA, and 10% ACN Mobile phase B (MPB) 10% water, 0.1% TFA, and 90% ACN

[0108] Reverse Phase Purification 1 (RP1): The crude product from Example 4A is dissolved in 90 wt% MPA and 10 wt% MPB. The solution is stirred for at least 7 hours to complete the decarboxylation of tryptophan. The aged crude solution is filtered and loaded onto a pre-equilibrated Kromasil 100-10-C8 packed column. The column is washed with a mixture of A buffer (90% water, 0.1% TFA, 10% ACN) and B buffer (10% water, 0.1% TFA, 90% ACN) to 30% ACN for 2 column volumes, and is prepared for elution by increasing the mixed concentration of ACN from 30% to 35% for 1 column volume. Tirzepatide is eluted from the column with increasing amounts of ACN at 1.5% per column volume until elution is complete. The eluate is fractionated and assayed for purity using RP-HPLC. Regenerate the column by increasing ACN from 47% to 65% for one column volume and continuing with 3 column volumes of 65% ACN. Re-equilibrate the column using 2 column volumes of 30% ACN before the next injection sequence.

[0109] Fractions eligible for mainstream inclusion are pooled. After all primary injections are complete, fractions that do not meet the purity criteria but are greater than 50% pure can be combined for recycle injection. The recycle fractions are separated into top and bottom fractions, diluted with Buffer A and stored refrigerated. The recycle injections are processed and pooled using the primary injection criteria, but only the main peak fractions are processed forward and not further recycled. Once the mainstream pool is complete, the intermediates are assayed for concentration and purity. Prior to RP2 processing, the material is diluted and the pH adjusted to pH 8. The RP1 process results in 37 kg crude product and 14277 g of contained product with an average pool purity of 90.9%.

[0110] Reverse-phase purification 2: The RP1 solution from Example 4A is loaded onto a pre-equilibrated Kromasil 100-10-C8 packed column. The column is filled with Buffer C (90% NH 4 OAc aqueous solution, pH 8.0, 10% ACN) and buffer D (10% NH 4Wash with a mixture of 100% ACN (aqueous OAc, pH 8.0, 90% ACN) to 2 column volumes of 20% ACN. Elute tirzepatide from the column with increasing ACN of 3.5% per column until elution is complete. Fractionate the eluate and assay for purity using RP-HPLC. After elution, regenerate the column by increasing ACN to 80% for 1 column volume and continuing with 3 column volumes of 80% ACN. Re-equilibrate the column with 2 column volumes of 20% ACN before the next injection sequence.

[0111] Fractions that qualify for mainstream inclusion are pooled. After all primary injections are complete, fractions that do not meet the purity criteria but are greater than 60% pure can be combined for recycle injection. The recycle fractions are split into front and back pools, diluted with Buffer C, and stored refrigerated. The recycle injections are processed and pooled using the primary injection criteria, but only the main peak fractions are processed forward and not further recycled. Once the mainstream pool is complete, the intermediates are assayed for concentration and purity. The pH of the material can be adjusted to 8.0 in preparation for the TFF step. The RP2 process starting with 14.2 kg results in 10.9 kg of inclusion product in 76.7% yield.

[0112] Ion Exchange Chromatography (IEX): The RP2 solution of Example 4A is filtered and loaded onto an Amberchrom CG-300M column. Two fractions are eluted using mobile phase E (10% aqueous ammonium acetate, 5% IPA, pH 8) and mobile phase F (isopropanol). Fractions are analyzed for peptide content and those below 3 mg / mL are discarded. Pooled fractions of concentrate are stored at 20° C. prior to precipitation. The IEX process starts with 10.9 kg of RP2 and results in 14.3 kg of Example 4A material-containing product with a purity of 97.8% pool purity.

[0113] Precipitation: The IEX solution of Example 4A (333 kg) is filtered and then charged with isopropanol (850 L) to reduce the water content to 10% w / w water or less. The diluted solution is cooled to 0±3° C. in preparation for MTBE charging and precipitation. MTBE (2304 L, 1708 kg) is cooled to 0±3° C. Cold MTBE is fed to the IEX solution at a rate of about 0.69 kg / min for about the first 37% of the MTBE charge. The feed rate is then increased to an average of about 2.3 kg / min to complete the remaining 63% of the MTBE charge. The temperature during the feed is maintained below 5° C. The resulting precipitation slurry is cold filtered (below −10° C.) and the filter cake is then washed with MTBE. The filter cake is dried to 2% LOD or less.

[0114] Humidification 4A: Humidify Example 4A by passing moist nitrogen through a filter dryer. Monitor the humidity of the gas stream exiting the filter outlet every 60 minutes. Continue humidification until no more than 0.5% MTBE and no more than 0.2% IPA remain in the wet cake. After completion of the humidification process, switch the nitrogen flow to flow dry nitrogen through the pure product cake of Example 4A. Sample the material for water and residual solvents for specific IPC targets and drying using dry nitrogen continues until the desired target moisture content of 5-7% w / w is met. A total of 12.9 kg of Example 4A is isolated with a purity of >95% peptide content. Overall yield based on Sieber resin loading = 31%.

[0115] Example 4B (Linear SPPS) Tirzepatide (SEQ ID NO: 1) [ka] [ka]

[0116] Preparation 23 The process for producing Preparation 23 is essentially as described in Example 4A, except that NMP is replaced entirely with DMF for all couplings and deprotections. Additionally, the stoichiometry of amino acid:Oxyma:DIC is reduced to 2.5:2.5:2.7 molar equivalents based on Sieber resin. The only exception related to the use of DMF is the coupling of Ile12 to Aib13, where NMP is retained. This example shows the process to 92.2 kg of Preparation 23 peptide on a resin intermediate of 17.6 kg of Sieber resin.

[0117] Preparation 24 The process substantially as described by Example 4A produces 92.1 kg of Preparation 23, and further processes 97.3 kg of Preparation 24 peptide on the resin intermediate. Preparation 24 is packaged and stored refrigerated (-20°C) prior to cleavage from the resin.

[0118] Resin cleavage and Example 4B crude isolation: Using conditions essentially as described in Example 4A, two batches are performed on a 32 kg scale of Preparation 24 to deliver 24.4 kg of Example 4B, 69.5% HPLC purity, 52.6% yield, and 21.3 kg of Example 4B, 88.3% HPLC purity, 45.2% yield. The crude intermediate is stored cold (-20°C) until purification.

[0119] Example 4B Purification: Crude Dissolution: Tirzepatide Example 4B crude is charged to a dissolution vessel and dissolved in 1:1 acetonitrile:water solution to a final concentration of the solution of 25 g solids / L. The pH of the resulting solution is adjusted to 8.5-9.5 with ammonium hydroxide to initiate the conversion of the depsipeptide isomers (10-15%) to Tirzepatide Example 4B. The pH adjusted mixture is stirred for at least 1 hour to allow the depsipeptide conversion to occur. Trifluoroacetic acid is then added to adjust the pH to 1.5-2.5 and diluted to 30% acetonitrile content in preparation for chromatography. In total, the crude solution is stirred for at least 7 hours to remove Trp CO 2 The salt is converted to tirzepatide Example 4B.

[0120] Conversion of Tirzepatide (TZP) to a Depsipeptide: [ka]

[0121] Conversion of depsipeptide to API: [ka]

[0122] Reverse Phase Purification 1 (RP1): The depsipeptide can be converted to API using the RP1 process substantially as presented by Example 4A. The RP1 purification process is substantially the same as described in Example 4A. However, the crude dissolution step described above enhances the functionality of the RP1 chromatography step. This allows for higher g Tirzepatide per L resin loading and reduces the number of injections required to purify crude Tirzepatide under the conditions described in Example 4. In this illustration, 23.7 kg of content-corrected crude Example 4B yields 25.4 kg Example 4B (107%) after RP1. Total solution volume = 2910 L @ 8.72 g / L, once all pooled fractions have been collected, the mixture is agitated, sampled, and retained prior to reverse phase purification 2 (RP2).

[0123] Reverse Phase Purification 2 (RP2): Substantially the same purification process as described in Example 4A, using methods known to those skilled in the art, is used for Reverse Phase Purification 2 (RP2). In this example, 15.2 kg containing Example 4B from RP1 is purified to 13.8 kg Example 4B with a purity of about 98% after RP2. Total solution volume = 808 L @ 17.0 g / L. The mixture is stored before tangential flow filtration.

[0124] Tangential Flow Filtration (TFF): Install the TFF membrane and flush with water. Prepare ammonium acetate buffer using low endotoxin purified water, acetic acid, and ammonium hydroxide. Then fill with isopropanol to make 5:95 100 mM NH4 OAc pH 8.0:IPA buffer is fed. The 17 g / L RP2 solution from Example 4B is concentrated through the TFF to approximately 125 g / L. The RP2 solution is recirculated, allowing the solvent to permeate the membrane while keeping the peptide solution in solution on the retentate side of the membrane. After concentration, diafiltration buffer is fed to the retentate holding tank while the permeate is continuously collected. Buffer exchange continues until the desired solvent composition and peptide concentration is met. The solution is emptied from the system and the resulting polarized layer is washed off the membrane and pooled with the peptide concentrate. Two sections of the RP2 solution (403.9 L @ 17 g / L, 9.87 kg API) are processed through the TFF.

[0125] Co-feed precipitation: Combine the TFF sections (138.2 kg, 78.3 g / L) and measure the KF (8.9%) to ensure water is less than 10%. Place MTBE (243 kg) in a separate vessel and cool to 0 °C. Add IPA (48 kg), water (6 kg), and MTBE (100 kg) to the precipitation vessel and cool the solution to 0 °C. The TFF and MTBE process streams are co-fed to the precipitation vessel at rates of 1.6-1.8 and 2.9-3.1 kg / min, respectively. Age the resulting slurry for an additional 0.7 h at 0 °C and then warm to 15 °C. Age the slurry for 1 h at 15 °C before adding MTBE (118 kg). Age the slurry for 1 h at 15 °C before cooling to 2.5 °C. Cold filter the slurry and wash the filter cake with MTBE (573 kg). Dry the filter cake to less than 2% LOD.

[0126] Moisturization: Moisturization substantially as shown by Example 4A is applied to the material of Example 4B using methods known to those skilled in the art. A total of 14.5 kg of Example 4B (SEQ ID NO: 1) is isolated with an HPLC purity of >97.7% and a peptide content of 88.4%. Overall yield based on Sieber resin loading = 46%.

[0127] Example 5 Continuous synthesis of preparation 31 using in-flow convergent chemistry The synthesis of preparation 31 from peptide fragments is carried out using both a batch approach to chemistry and sequential addition of the fragments in a tubular flow reactor. A generalized approach to the synthesis involves coupling of the two fragments by blending the two solutions in a tubular reactor with the coupling agent, followed by the addition of base and an extended residence time in the tubular reactor to effect removal of the FMOC protecting group. This prepares the coupled species for the addition of the next fragment. Excess reagents, base, and solvent are removed between successive coupling reactions using nanofilters with membranes sized to retain the peptide and permeate low molecular weight impurities. Diafiltration is used to completely remove low molecular weight impurities before the subsequent coupling step. Descriptions and analytical results from examples of these transformations are provided below.

[0128] Use HPLC to confirm the synthesis of Preparation 31 from Preparation 29 and Preparation 30. The analytical method uses a (2.1 mm ID x 150 mm x 1.7 micron particle size) C4 stationary phase column at 65 °C with a 60-98% B gradient of 0.1% TFA in water and acetonitrile over 12 minutes. UV detection at 214 nm is used for this material.

[0129] Table A.5 shows the high resolution mass spectrometry data collected on the product of the coupling reaction of step 3 made on-stream (Preparation 31). The mass accuracy confirms the species of interest. [Table 16] Table A.5 Confirmation of measured preparation 31 with mass accuracy calculated using high resolution mass spectrometry data.

[0130] Native chemical ligation is a process that is useful for preparing full-length peptides that contain cysteine ​​or alanine in the sequence. This process utilizes the chemoselective reaction of two unprotected peptide segments to generate a temporary thioester-linked intermediate. The thioester-linked intermediate rearranges to provide a full-length ligation product with a native peptide bond at the ligation site. Those skilled in the art will understand that the technique of native chemical ligation can be useful for the chemical synthesis of full-length peptides that contain cysteine ​​or alanine.

[0131] Example 6 Native Chemical Ligation Process SEQ ID NO:1 [ka]

[0132] Synthesis of Fmoc-hydrazine-CTC resin (Preparation 32) 2-CTC resin (10.7 g, 17.7 mmol) is swelled in 100 mL of DCM at 0 °C for 20 min. 9-Fluorenylmethyl carbazate (15.6 g, 61.4 mmol, 3.5 equiv.) is dissolved in 210 mL of 2:1 DMF:DCM. DIEA (31 mL, 178 mmol, 10.1 equiv.) is added to the 9-Fluorenylmethyl carbazate solution. This solution is then added slowly to the resin at 0 °C. Stir at 0 °C for approximately 1 h and allow to warm to room temperature. The reaction mixture is stirred at room temperature for 16 h. Methanol (10 mL) is then added to quench the remaining 2-CTC resin and stirred for 15 min. The resin is rinsed with 200 mL of DMF, followed by DMF (2x100 mL), water (3x100 mL), DMF (3x100 mL), methanol (3x100 mL) and finally DCM (3x100 mL). The resin is dried in a vacuum oven at 27°C for 16 hours. The loading of the resin is determined by quantitative NMR to be 0.74 mmol / g. [ka]

[0133] Synthesis of peptide hydrazide (17-mer) (Preparation 33 SEQ ID NO:32 Hydrazine-CTC resin (1.01 g, loading value: 0.65 mmol / g) is placed in a 40 mL reaction vessel and swollen on the peptide synthesizer with 3x4 mL DCM (30 s each) followed by 2x10 mL DMF (20 min each). Dissolve Fmoc-Ile-OH (0.919 g, 2.60 mmol, 4 eq.) and HBTU (0.99 g, 2.61 mmol, 4 eq.) in 7 mL DMF. Add DIPEA (0.91 mL, 5.22 mmol, 8 eq.) to the amino acid solution and make the volume to 10 mL with DMF. Add the activated amino acid solution to the resin. Mix the slurry with nitrogen for 8 h. After 8 h, wash the resin with 5x10 mL DMF, 5x10 mL DCM and dry for 12 h. The loading of the resulting resin is determined to be 0.54 mmol / g by quantitative NMR. 0.91 g of this resin is used for the synthesis of preparation 33 (SEQ ID NO:32).

[0134] Deprotection: 4x9mL of 20% v / v piperidine in DMF, 30 min each.

[0135] Coupling: 3 equivalents of amino acid, 3 equivalents of OXYMA and 3.3 equivalents of DIC are used for amino acid coupling. After each coupling and final iteration of deprotection, N 2 Wash the resin with 5 x 9 mL of DMF for 1 min with mixing. After peptide hydrazide synthesis, 2 Wash the resin with DCM with mixing. Allow the resin to dry on the synthesizer.

[0136] Deprotection and cleavage: 25 mL of cleavage cocktail made with 5% w / v dithiothreitol (DTT), 2.5% v / v water, 2.5% v / v triisopropylsilane (TIPS), and 90% trifluoroacetic acid (TFA) is added to the dried resin (2.37 g) and mixed on a rotary mixer for 3 h. The resin is filtered and washed with 2x2.5 mL of TFA. The filtrate is poured into 175 mL of cold MTBE and the peptide is immediately precipitated. The filtration flask is washed with 2x2.0 mL of TFA and poured into cold MTBE. After cooling to -20 °C for 30 min, it is centrifuged. The peptide precipitate is then washed twice with 150 mL of MTBE and centrifuged. The peptide precipitate is dried in a vacuum oven at 27 °C for 16 h. A 1.25 g sample of crude preparation 33 is obtained after drying [expected (mass + 2H + ) / 2=968.4883, observed value (mass + 2H + ) / 2=968.4879]. [ka]

[0137] Approximately 0.62 mmol of preparation 34 is synthesized on Sieber amide resin by standard SPPS protocols. Fmoc-Lys(ivDde)-OH is used for orthogonal deprotection and lysine acylation.

[0138] Deprotection of ivDde: Dilute hydrazine monohydrate (64% w / w) (1.98 g, 25.3 mmol) to 24.4 g with DMF and add 20 g to the resin. Agitate the slurry with a stream of nitrogen. After about 2 hours, wash with 5x9 mL of DMF. Repeat once more.

[0139] Dissolve 2-[2-[2-[[2-[2-[2-[[(4S)-5-tert-butoxy-4-[(20-tert-butoxy-20-oxo-icosanoyl)amino]-5-oxo-pentanoyl]amino]ethoxy]ethoxy]acetyl]amino]ethoxy]ethoxy]acetic acid (1094.4 mg, 1.252 mmol, 2 equiv.) in 10 mL of anhydrous DMF. Add TNTU (506.9 mg, 1.360 mmol, 2.2 equiv.) and DIEA (0.24 mL, 1.4 mmol, 2.2 equiv.). Bring the volume to 15 mL with anhydrous DMF. Mix on a rotary mixer for 30 min. Then add the activated ester of preparation 6 to the resin and mix with a nitrogen stream for 12 h. After 12 h, drain the solution and centrifuge with N 2 Wash the resin with 5 x 10 mL of DMF and 7 x 10 mL of DCM for 1 min with mixing. Allow the resin to dry on the synthesizer for 8 h.

[0140] Deprotection and cleavage: 20 mL of cleavage cocktail made of 5% w / v dithiothreitol (DTT), 2.5% v / v water, 2.5% v / v triisopropylsilane (TIPS) and 90% trifluoroacetic acid (TFA) is added to the dried resin (2.42 g) and mixed on a rotary mixer for 3 h. The resin is filtered and washed with 2x2.0 mL of TFA. The filtrate is poured into 200 mL of cold MTBE and the peptide is immediately precipitated. The filtration flask is washed with 2x2 mL of TFA and poured into cold MTBE. Cool to -20 °C for 30 min and then centrifuged. The peptide precipitate is washed twice with 240 mL of MTBE and centrifuged. The peptide precipitate is dried in a vacuum oven at 27 °C for 14 h. After drying, 1.853 g of crude preparation 34 is obtained. Purify by RP-HPLC on a Kromasil 100-10-C8 10 μm column (30 mm x 250 mm) at ambient temperature. After an initial 5 min of 15% acetonitrile in water, a linear gradient of 30-55% acetonitrile in water over 25 min, with a constant 0.1% TFA for 30 min is used. 1.28 g of purified preparation 34 (SEQ ID NO: 33) is obtained [expected (mass + 2H + ) / 2=1470.7929, observed value (mass + 2H + ) / 2=1470.7885].

[0141] Thioester synthesis (conversion of preparation 33 to preparation 35) Dissolve the crude peptide hydrazide (Preparation 33, 2.422 g, 1.251 mmol) in 50 mL of ligation buffer (6 M guanidine hydrochloride and 0.2 M disodium hydrogen phosphate monobasic, pH 3.35) and cool to -15 °C in an acetone-ice bath. Add 9.4 mL of 1 M sodium nitrite solution (9.4 mmol, 7.5 equiv.) to the peptide hydrazide solution and stir at -15 °C for 20 min. Meanwhile, bring 1 mL of 2,2,2-trifluoroethanethiol (TFET) up to 10 mL with ligation buffer (6 M guanidine hydrochloride and 0.2 M disodium hydrogen phosphate monobasic, pH 7.0). After 20 min, add 10 mL of the TFET mixture to the peptide hydrazide solution to trigger in-situ thiolysis of the peptidyl azide generated from Preparation 33. [ka]

[0142] The pH of the reaction mixture is adjusted to approximately 6.95 with 5N sodium hydroxide solution. Thiolysis of the peptidyl azide is carried out for 45 min and the volume is made up to 100 mL with ligation buffer (pH 7.0). The crude thioester mixture is purified by RP-HPLC on a Waters X-BridgeC18 10 μm column (10 mm x 250 mm) at ambient temperature. After the first 2.8 min of 10% acetonitrile in water, a linear gradient is used from 25 to 42% acetonitrile in water over 25 min, with 0.1% TFA constant throughout the 28 min purification. This gives 1.03 g of TFET thioester (Preparation 35 (SEQ ID NO: 34)) [expected (mass + 2H + ) / 2=1010.4650, observed value (mass + 2H + ) / 2=1010.4620].

[0143] Native Chemical Ligation: An aqueous solution of 6 M guanidine hydrochloride and 0.3 M disodium hydrogen phosphate monobasic (pH 7.0) is the ligation buffer used in native chemical ligation. All solutions are made in this ligation buffer. Dissolve 350.4 mg (0.174 mmol) of peptide thioester preparation 35 (SEQ ID NO: 34) in 50 mL of ligation buffer. Add 8.0 mL of 0.5 M 4-mercaptophenylacetic acid (MPAA) solution to the peptide thioester solution. Dissolve the N-terminal cysteine-containing peptide (Preparation 34 (SEQ ID NO: 33), 524.6 mg, 0.178 mmol, 1.03 equiv.) in 48 mL of ligation buffer in a 50 mL centrifuge tube. Add the solution of Preparation 34 to the thioester solution. Rinse the centrifuge tube with 2x8 mL of ligation buffer (approximately pH 7.0) and add to the reaction mixture. The pH of the reaction mixture is adjusted to about 7 with 5N NaOH solution. 8.0 mL of tris(2-carboxyethyl)phosphine (TCEP, 0.5 M, pH 7.0) is added to the reaction mixture and the pH is adjusted again to 7.0 with 0.2 mL of 5N sodium hydroxide solution. The reaction is stirred at room temperature for 24 h and then stored in the freezer. An additional 3 mL of 0.5 M TCEP solution is added before purification. Purification of preparation 36 (SEQ ID NO: 35) is performed by RP-HPLC at ambient temperature on a Kromasil C18 10 μm column (10 mm × 250 mm) with a linear gradient of 10% acetonitrile in water for the first 4 min, 20 to 50% acetonitrile in water over 23 min (titrated to 0.1% acetic acid and pH 9.0) during the 28 min purification. Approximately 372 mg (44.3%) of tirzepatide cysteine ​​analog preparation 36 is obtained after purification [expected value (mass + 3H + ) / 3=1615.17263, observed value (mass + 3H + ) / 3=1615.1686]. [ka]

[0144] Desulfurization: An aqueous solution of 6-guanidine hydrochloride and 0.3 M disodium hydrogen phosphate monobasic (pH 7.0) is the buffer used for desulfurization. All solutions are made up in this buffer. Dissolve 2,2'-azobis[2-(2-imidazolin-2-yl)propane] dihydrochloride (Preparation 37, 808.2 mg, 2.5 mmol) in 10 mL of buffer and adjust the pH to about 7.0 with 5 N NaOH. Bring the volume to 15 mL with buffer. Dissolve tirzepatide cysteine ​​analogue Preparation 36 (105.2 mg, 0.022 mmol) in 30 mL of buffer and add 6 mL of Preparation 37 solution to it. Add 5 mL of 0.3 M L-glutathione reducing solution (L-GSH, pH 7.0) and 7.5 mL of 0.5 M TCEP solution (pH 7.0). The solution is heated at 44 °C for 4.5 h, and UPLC analysis indicates the reaction is complete [expected (mass + 3H + ) / 3=1604.5153, observed value (mass + 3H + ) / 3=1604.5122]. The desulfurization yield is calculated by UPLC using tirzepatide (SEQ ID NO: 1) reference standard. The yield is estimated to be 47%. [ka]

[0145] Native Chemical Ligation (Approach 2): Synthesis of Peptide Hydrazide Preparation 39 SEQ ID NO:36 Hydrazine-CTC resin (2.03 g, 1.32 mmol, loading value: 0.65 mmol / g) is placed in a 40 mL reaction vessel and swelled with 3x10 mL DCM (30 s each) followed by 2x10 mL DMF (20 min each) on a Symphony synthesizer. Dissolve HBTU (1.48 g, 3.90 mmol, 3.0 equiv.) in 13.1 mL of (25S,52S)-52-((((9H-fluoren-9-yl)methoxy)carbonyl)amino)-25-(tert-butoxycarbonyl)-2,2-dimethyl-4,23,28,37,46-pentaoxo-3,32,35,41,44-pentaoxa-24,29,38,47-tetraazatripentacontan-53-oic acid (Preparation 17, 365 mg / mL in DMF) solution (3.91 mmol, 3.0 equiv.). Add DIPEA (1.4 mL, 8.04 mmol, 6.1 equiv.) to the above solution and make the volume to 19 mL with DMF. Mix the solution on a rotary mixer at room temperature for 30 min. The activated ester solution of Preparation 17 is added to the resin. The slurry is mixed with nitrogen for 8 hours. After 8 hours, the resin is washed with 5x10 mL DMF, 5x10 mL DCM and dried for 12 hours. The resulting resin loading is determined to be 0.26 mmol / g by quantitative NMR. 1.82 g of this resin is used for the synthesis of peptide hydrazide preparation 39 (SEQ ID NO:36).

[0146] Deprotection: 4x9mL of 20% v / v piperidine in DMF, 30 min each.

[0147] Coupling: 3 equivalents of amino acid, 3 equivalents of OXYMA and 3.3 equivalents of DIC are used for amino acid coupling.

[0148] After each coupling and final deprotection iteration, N 2 Wash the resin with 5 x 9 mL of DMF for 1 min with mixing. After peptide hydrazide synthesis, 2 Wash the resin with 7 x 10 mL of DCM for 1 min with mixing. The resin is then dried on the synthesizer for approximately 12 h.

[0149] Deprotection and cleavage: 25 mL of cleavage cocktail made of 5% w / v dithiothreitol (DTT), 2.5% v / v water, 2.5% v / v triisopropylsilane (TIPS), and 90% trifluoroacetic acid (TFA) is added to the dried resin and mixed on a rotary mixer. The resin is filtered, washed with TFA (2x2.5 mL), and the filtrate is poured into 175 mL of cold MTBE. The filtration flask is washed with TFA (2x2.5 mL), and the washes are poured into cold MTBE. Cool to -20 °C for 30 min and then centrifuged. The peptide precipitate is then washed twice with 150 mL of MTBE and centrifuged. The peptide precipitate is dried in a vacuum oven at 27 °C for 16 h. After drying, 1.70 g of crude peptide hydrazide preparation 39 (SEQ ID NO: 36) is obtained. The crude peptide hydrazide, Preparation 39, is purified by RP-HPLC on a Waters XSelectCSHC18 10 μm column (10 mm x 250 mm) at ambient temperature using a linear gradient of 10% acetonitrile in water for the first 3 min, followed by 20-55% acetonitrile in water over 23 min, with 0.1% TFA constant throughout the 28 min purification. Approximately 110 mg of partially purified hydrazide Preparation 39 is obtained.

[0150] Deprotection and cleavage: The dried resin (2.92 g) is mixed with 25 mL of cleavage cocktail made of 5% w / v dithiothreitol (DTT), 2.5% v / v water, 2.5% v / v triisopropylsilane (TIPS), and 90% trifluoroacetic acid (TFA) on a rotary mixer. The resin is filtered and washed with 2x2.5 mL of TFA. The filtrate is poured into 200 mL of cold MTBE and the peptide is immediately precipitated. The filtration flask is then washed with 2x2 mL of TFA and the washings are poured into cold MTBE. After cooling to -20 °C for 30 min, it is centrifuged. The peptide precipitate is then washed twice with 240 mL of MTBE and centrifuged. The peptide precipitate is then dried in a vacuum oven at 27 °C for 16 h. Approximately 1.7 g of crude 19-mer preparation 40 (SEQ ID NO: 37) is obtained.

[0151] Native chemical ligation: An aqueous solution of 6 M guanidine hydrochloride and 0.3 M disodium hydrogen phosphate monobasic (pH 7.0) is the ligation buffer used in native chemical ligation. All solutions are made in this ligation buffer. Dissolve the partially purified peptide hydrazide (preparation 39, 56 mg, 0.019 mmol) in 5 mL of ligation buffer (6 M guanidine hydrochloride and 0.3 M disodium hydrogen phosphate monobasic, pH 3.35) and cool to -15 °C in an acetone-ice bath. Add 0.25 mL of 1 M sodium nitrite solution (0.25 mmol, 13.2 equiv.) to the peptide hydrazide solution and stir at -15 °C for 10 min. After 10 min, 0.8 mL of 0.5 M 4-mercaptophenylacetic acid (MPAA) solution is added to the peptide hydrazide solution to cause in-situ thiolysis of the peptidyl azide generated from preparation 39. The pH of the reaction mixture is adjusted to about 7.0 with 5 N sodium hydroxide solution. Thiolysis of the peptidyl azide is carried out for 30 min. [ka]

[0152] Approximately 0.62 mmol of preparation 40 (SEQ ID NO: 37) is synthesized on Sieber mide resin using standard SPPS protocols. N-terminal cysteine-containing preparation 40 (26.1 mg, 0.014 mmol, 0.74 quiv) is dissolved in 1 mL of ligation buffer. The solution of preparation 40 is added to the thioester solution. The vial containing preparation 40 is rinsed with 1 mL of ligation buffer (pH 7.0) and added to the reaction mixture. After 15 min, 1.0 mL of tris(2-carboxyethyl)phosphine (TCEP, 0.5 M, pH 7.0) is added to the reaction mixture and the pH is adjusted to 7.0 with 5 N sodium hydroxide solution. The reaction is stirred at room temperature for 1 h. Tirzepatide cysteine ​​analog preparation 42 is observed in the reaction mixture. [ka]

[0153] array SEQ ID NO:1 Tirzepatide YX1EGTFTSDYSIX2LDKIAQKAFVQWLIAGGPSSGAPPPS In the formula, X 1 is Aib, and X 2 is Aib, and K at the 20th position is (2-[2-(2-amino-ethoxy)-ethoxy]-acetyl) 2 -(γGlu) 1 -CO-(CH 2 ) 18 -CO 2 Chemically modified through attachment of H to the epsilon-amino group of the K side chain, and the C-terminal amino acid is amidated as a C-terminal primary amide SEQ ID NO:2 [ka] SEQ ID NO:3 [ka] SEQ ID NO:4 [ka] SEQ ID NO:5 [ka] SEQ ID NO:6 [ka] SEQ ID NO:7 [ka] SEQ ID NO:8 [ka] SEQ ID NO:9 [ka] SEQ ID NO:10 [ka] SEQ ID NO:11 [ka] SEQ ID NO:12 [ka] SEQ ID NO:13 [ka] SEQ ID NO:14 [ka] SEQ ID NO:15 [ka] SEQ ID NO:16 [ka] SEQ ID NO:17 [ka] SEQ ID NO:18 [ka] SEQ ID NO:19 [ka] SEQ ID NO:20 [ka] SEQ ID NO:21 [ka] SEQ ID NO:22 [ka] SEQ ID NO:23 [ka] SEQ ID NO:24 [ka] SEQ ID NO:25 [ka] SEQ ID NO:26 [ka] SEQ ID NO:27 [ka] SEQ ID NO:28 [ka] SEQ ID NO:29 [ka] SEQ ID NO:30 [ka] SEQ ID NO:31 [ka] SEQ ID NO:32 [ka] SEQ ID NO:33 [ka] SEQ ID NO:34 [ka] SEQ ID NO:35 [ka] SEQ ID NO:36 [ka] SEQ ID NO:37 [ka] SEQ ID NO:38 [ka] SEQ ID NO:39 [ka] SEQ ID NO:40 [ka]

Claims

1. Compound of SEQ ID NO:4: 【Chemistry 1】 or a pharma- ceutically acceptable salt thereof.

2. Compound of SEQ ID NO: 12: 【Chemistry 2】 or a pharma- ceutically acceptable salt thereof.

3. Compound of SEQ ID NO: 19: 【Chemistry 3】 or a pharma- ceutically acceptable salt thereof.

4. Compound of SEQ ID NO:30: 【Chemistry 4】 or a pharma- ceutically acceptable salt thereof.

5. Compound of SEQ ID NO:32: 【Chemistry 5】 or a pharma- ceutically acceptable salt thereof.

6. Compound of SEQ ID NO:34: 【Chemistry 6】 or a pharma- ceutically acceptable salt thereof.

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