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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 862120생성일: 2026년 10월 25일

Bicyclo[2.2.1]heptane-1-methanesulfonic acid, 7,7-dimethyl-2-oxo-, (1S)- → (3R*,4S*,5S*,6S*)-N,N-Diethyl-5-(2,5-dimethoxybenzylamino)-6-diphenylmethyl-1-azabicyclo[2.2.2]octane-3-carboxamide

https://huagongshe.com/reaction/862120

반응식

참여 물질

역할이름HCID투입량
반응물Bicyclo[2.2.1]heptane-1-methanesulfonic acid, 7,7-dimethyl-2-oxo-, (1S)-HCID 18462—
반응물2,5-DimethoxybenzenemethanamineHCID 18652—
반응물Sodium triacetoxyborohydrideHCID 5049666—
반응물(3R*,4S*)-N,N-Diethyl-6-diphenylmethyl-5-oxo-1-azabicyclo[2.2.2]octane-3-carboxamideHCID 53867570—
용매Acetic AcidHCID 176—
용매WaterHCID 962—
용매TolueneHCID 1140—
생성물(3R*,4S*,5S*,6S*)-N,N-Diethyl-5-(2,5-dimethoxybenzylamino)-6-diphenylmethyl-1-azabicyclo[2.2.2]octane-3-carboxamideHCID 5726320644%

반응 단계

A mixture of 23 (3.9 g, 10 mmol), 2,5-dimethoxybenzyl amine (1.9 g, 11 mmol) (Acta. Chem. Scand., 25. p. 2629 (1971)) and camphor sulfonic acid (120 mg) in toluene (40 ml) was heated at reflux with removal of water for 8 hours and then the solvent was removed. The residue was dissolved in small amount of THF (c.a. 5 ml) and this solution was added to a solution of sodium triacetoxyborohydride (5.3 g, 25 mmol) in acetic acid (100 ml) at room temperature. The mixture was stirred at room temperature for 4 hours and the solvent was removed. Water (25 ml) was added and the mixture was neutralized with NaHCO3 and extracted with EtOAc three times. The clude was purified by recrystallization from EtOAc to give 24 (2.4 g, 4.4 mmol, 44%).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05716965
출처 데이터셋uspto-grants-1998_02
ORD IDord-c376f54116164601bb3cb227d3bc7c41
출처 메모uspto-grants-1998_02