Octahydro-1h-pyrrolo[2,3-c]pyridine derivatives and octahydro-1h-pyrrolo[3,2-c]pyridine derivatives and preparation methods thereof
A derivative, pyrrole technology, applied in the field of chemistry, can solve the problems of long preparation routes, harsh conditions, and expensive starting materials
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Embodiment 1
[0075] Embodiment 1: Preparation 1-benzyl-4-cyanomethyl-3-oxo-piperidine-4-carboxylic acid ethyl ester
[0076]
[0077]The raw material N-benzyl-3-oxo-piperidine-4-carboxylic acid ethyl ester (A, 383g, 1.47mol) was dissolved in 1000mL acetone, and potassium carbonate solid (284g,, 2.06mol, 1.4eq ), bromoacetonitrile (212g, 1.77mol, 1.2eq), N2 protection, stirring at room temperature for 2 days. After filtration, washing with ethyl acetate, concentration, the crude product was separated and purified by silica gel column chromatography to obtain 351 g of product (B), yield: 80%. 1H NMR (400MHz, CDCl3) δppm=7.27~7.16(m,5H), 4.19~4.17(q,2H), 3.52~3.48(dd,2H), 3.20~3.01(dd,2H), 2.69~2.63(br ,5H), 1.19~1.15(m,3H), 1.83~1.78(br,1H). MS-ESI(+):cal.300; found: 301(M+H), 333(M+Na).
Embodiment 2
[0078] Embodiment 2: Preparation of 6-benzyl-octahydro-pyrrolo[2,3-c]pyridine-3a-carboxylic acid ethyl ester
[0079]
[0080] Compound (B) (90 g, 0.3 mol) was dissolved in 500 mL of dioxane, added Raney nickel (90 g), and hydrogenated at 60° C. for 3 days. The Raney nickel was removed by direct filtration, concentrated directly, and the crude product was separated and purified by silica gel column chromatography to obtain 64 g of product (C), yield: 74%. The solid was directly carried on to the next reaction. 1 h NMR (400MHz, CDCl 3 )δppm=7.31~7.16(m,5H),4.91(br,2H),4.15~4.09(t,2H),3.66~3.22(m,4H),3.01~2.99(br,1H),2.63~2.61( br,1H), 2.41~2.38(dd,1H), 2.16~1.83(m,4H), 1.61(br,1H), 1.21~1.14(dd,3H).MS-ESI(+):cal.288; found: 289(M+H).
Embodiment 3
[0081] Embodiment 3: Preparation of 6-benzyl-hexahydro-pyrrolo[2,3-c]pyridine-1,3a-dicarboxylic acid-1-tert-butyl-3a-ethyl ester
[0082]
[0083] Compound (C) (64g, 0.22mol) was dissolved in 400mL of dichloromethane, added triethylamine (48mL, 1.5eq), Boc2O (64g, 1.05eq), reacted overnight at room temperature, washed with crushed ice with 2N dilute hydrochloric acid until neutral , washed with dichloromethane and brine, dried, filtered and concentrated, the crude product was separated and purified by silica gel column chromatography to obtain 74g of product (D), yield: 87%. 1H NMR (400MHz, CDCl3) δppm=7.23~7.16(m,5H), 4.31~4.09(br,3H), 3.56~3.29(m,4H), 3.01~2.93(br,1H), 2.61~2.51(br ,1H), 2.08~1.99(br,1H), 1.84~1.70(br,1H), 1.45~1.17(m,13H).MS-ESI(+):cal.388;found:411(M+Na) , 289 (M-Boc+H).
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