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Method for efficiently preparing carfilzomib

A carfilzomib and reaction technology, which is applied in the preparation field of carfilzomib, can solve the problems of reduced yield of target product, mild reaction conditions, high compound price, etc., and achieves excellent atom economy, small molecular weight, and easy operation. simple effect

Active Publication Date: 2021-05-25
JIANGXI NORMAL UNIVERSITY
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  • Abstract
  • Description
  • Claims
  • Application Information

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Problems solved by technology

However, the dipeptides formed by the condensation of compound (II) and other amino acids are all unstable in the amine obtained after removing the amino protecting group, and the price of compound (II) is expensive
Therefore, the right-to-left strategy for synthesizing carfilzomib is not dominant. Most of the existing reports on the synthesis of carfilzomib are carried out using a left-to-right strategy, but some of these methods have mild reaction conditions, and some operations Complicated (anhydrous condition is required) and the yield is low, such as the patent application number 201410343409.3, the patent application number 201410135563.1, the patent application number 200880119013.3 and the U.S. patent US2005 / 0245435AI. The overall yields of Zomi's method were less than 45%
In addition, the strategy of synthesizing carfilzomib from left to right also involves the activation of long-chain polypeptide carboxylic acids. Traditional condensing agents are not a problem when activating amino-protected single amino acids. However, when activating long-chain polypeptide carboxylic acids , the chiral carbon at the α position of the carboxyl group will undergo serious racemization, resulting in a decrease in the yield of the target product and difficulty in separation

Method used

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  • Method for efficiently preparing carfilzomib
  • Method for efficiently preparing carfilzomib
  • Method for efficiently preparing carfilzomib

Examples

Experimental program
Comparison scheme
Effect test

preparation Embodiment 1

[0094] Synthesis of chloroacetic acid activated ester (E1):

[0095]

[0096] Add chloroacetic acid (5mmol), phenyl allenone (10mmol) and 1,2-dichloroethane (DCE, 10mL) into a clean round-bottomed flask, stir the reaction at 35°C, and track and monitor using TLC, The reaction was complete in 10 hours. After the reaction, the system solution was concentrated and purified by column chromatography to obtain chloroacetic acid activated ester (4.7 mmol) as a light yellow solid with a yield of 94%.

[0097] 1 H NMR (400MHz, CDCl 3)δ7.92(d, J=7.5Hz, 2H), 7.56(t, J=7.4Hz, 1H), 7.47(t, J=7.6Hz, 2H), 6.85(s, 1H), 4.22(s, 2H), 2.42(s, 3H);

[0098] 13 C NMR (100MHz, CDCl 3 )δ190.0, 164.7, 162.7, 138.3, 133.1, 128.6, 128.2, 114.0, 40.8, 18.5.

preparation Embodiment 2

[0100] Synthesis of Coupling Product A:

[0101]

[0102] In a clean round bottom flask, add the activated chloroacetic acid ester (4.5mmol) prepared in Preparation Example 1, H 2 N-HomoPhe-O t Bu (5.4mmol) and N,N-dimethylformamide (DMF, 10mL), the reaction was stirred at room temperature and tracked and monitored by TLC. The reaction was complete within 15min. After the reaction, transfer the reaction solution to a separatory funnel, add water, then add ethyl acetate for extraction, extract three times with ethyl acetate and combine the organic phases, the combined organic phases are dried with anhydrous magnesium sulfate and filtered , the dried organic phase was concentrated and then separated and purified by column chromatography to obtain coupling product A (4.275 mmol), a white solid, with a yield of 95%.

[0103] 1 H NMR (400MHz, CDCl 3 )δ7.25–7.16(m,2H),7.16–7.06(m,3H),7.03(d,J=7.9Hz,1H),4.54–4.44(m,1H),3.94(s,2H),2.67 –2.48(m,2H),2.22–2.08(m,1H),2.03–1.89(m,1...

preparation Embodiment 3

[0106] Synthesis of activated ester E2:

[0107]

[0108] Add coupling product A (4.2mmol), dichloromethane (10mL) and trifluoroacetic acid (10mL) prepared in Preparation Example 2 to a clean round bottom flask, stir at room temperature, and detect by TLC and LC-Ms , The reaction is completed in about 1h. Then, after removing dichloromethane and trifluoroacetic acid under vacuum, add ethyl acetate to the round bottom flask and transfer to a separatory funnel, then add water, extract three times with ethyl acetate and combine the organic phases, the combined organic phases After drying with anhydrous magnesium sulfate and filtering, the dried organic phase was concentrated in vacuo to remove ethyl acetate, and then phenylketene (5 mmol) and 1,2-dichloroethane (DCE, 10 mL ), the reaction was stirred at 35° C., and monitored by TLC, and the reaction was complete in about 15 hours. After the reaction, the solution in the reaction system was concentrated under vacuum and separ...

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Abstract

The invention provides a method for efficiently preparing carfilzomib, which comprises the following steps: by taking chloroacetic acid, homophenylalanine, phenylalanine, leucine and (2S)-2-amino-4-methyl-1-[(2R)-2-methyl oxiranyl]-1-pentanone trifluoroacetate as raw materials and phenyl allene ketone as a condensation reagent, carrying out a condensation reaction to obtain carfilzomib; carrying out step-by-step coupling condensation through the steps of carboxylic acid activation, condensation, carboxyl protecting group removal and the like to obtain an intermediate product, and then carrying out catalytic condensation reaction on the intermediate product and morpholine to obtain a target compound. The condensing agent used in the method has the advantages of simplicity in preparation, small molecular weight and no racemization when the chiral carboxylic acid is activated. Meanwhile, the method is mild in reaction condition and simple to operate, the total yield is up to 68-72%, and the method has excellent atom economy and is a novel, efficient and very practical synthesis method of carfilzomib.

Description

technical field [0001] The invention relates to the preparation of carfilzomib, in particular to a new method for efficiently preparing carfilzomib by using allenone condensing agents, and belongs to the technical field of pharmaceutical synthesis chemistry. Background technique [0002] Carfilzomib, the English name is Carfilzomib, and its structural formula is as follows. It is a second-generation protease inhibitor administered intravenously. On July 20, 2012, the U.S. Food and Drug Administration (FDA) approved the listing of the product Carfilzomib (Carfilzomib) freeze-dried powder for injection produced by Onyx Pharmaceuticals Inc of the United States, and it is used to treat refractory multiple myeloma. The inhibitory effect of carfilzomib on protease is more durable and irreversible, and the possibility of drug resistance in patients is low, and the side effects are small, so it has attracted extensive attention from the medical, pharmaceutical and even chemical ci...

Claims

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Application Information

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IPC IPC(8): C07K7/06
CPCC07K7/06Y02P20/55
Inventor 赵军锋王雪伟汪正宁
Owner JIANGXI NORMAL UNIVERSITY
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