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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 862124생성일: 2026년 10월 25일

Sodium Hydroxide → (2R*,4S*,5S*,6S*)-N,N-dimethyl-5-(2,5-dimethoxybenzyl)amino-6-diphenylmethyl-1-azabicyclo[2.2.2]octane-2-carboxamide

https://huagongshe.com/reaction/862124

반응식

참여 물질

역할이름HCID투입량
반응물Sodium HydroxideHCID 14798—
반응물2,5-DimethoxybenzenemethanamineHCID 18652—
반응물Sodium triacetoxyborohydrideHCID 5049666—
반응물(2R*,4S*,6S*)-N,N-dimethyl-5-oxo-6-diphenylmethyl-1-azabicyclo[2,2,2]octane-2-carboxamideHCID 70114993—
촉매Bicyclo[2.2.1]heptane-1-methanesulfonic acid, 7,7-dimethyl-2-oxo-, (1S)-HCID 18462—
용매Acetic AcidHCID 176—
용매WaterHCID 962—
용매TolueneHCID 1140—
용매TetrahydrofuranHCID 8028—
생성물(2R*,4S*,5S*,6S*)-N,N-dimethyl-5-(2,5-dimethoxybenzyl)amino-6-diphenylmethyl-1-azabicyclo[2.2.2]octane-2-carboxamideHCID 7011464770.1%

반응 단계

A mixture of compound 34 (2.22 g, 6.13 mmole), 2,5-dimethoxybenzylamine (1.23 g, 7.36 mmole) and CSA (camphersulfonic acid) (20 mg) in toluene (50 ml) was heated at reflux for 24 hours with Dean Stark water separator. The solvent was removed under reduced pressure. The crude imine was used to the next step without purification. A solution of the crude imine in dry THF (20 ml) was added to a solution of NaBH(OAc)3 (3.9 g, 18.4 mmole) and acetic acid (3 ml) in dry THF (20 ml) at 5° C. and stirred at room temperature for 15 hours. The pH value was adjusted to pH=10 by 1N NaOH, and extracted with EtOAc (20 ml×3). The combined organic extracts were washed with brine, dried over MgSO4 and concentrated down. The crude oil was purified by silica gel chromatography (EtOAc:Hexane=1:1 as eluent) to give colorless oil. The oil was purified by recrystallization from MeOH to give compound 35 as colorless crystal (2.21 g, 4.3 mmole, 70%).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05716965
출처 데이터셋uspto-grants-1998_02
ORD IDord-b7009d613280405ca03aed37cc57ee2e
출처 메모uspto-grants-1998_02