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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 734321생성일: 2026년 10월 23일

1,2-Dichloroethane → 1-Benzyl-4-(1-tert-butoxycarbonyl-piperidine-4-carbonyl)-[1,4]-diazepane

https://huagongshe.com/ko/reaction/734321

반응식

참여 물질

역할이름HCID투입량
반응물1,2-DichloroethaneHCID 11—
반응물1-HydroxybenzotriazoleHCID 75771—
반응물1-Benzyl-1,4-diazepaneHCID 228365—
반응물1-(tert-Butoxycarbonyl)-4-piperidinecarboxylic acidHCID 392871—
용매DichloromethaneHCID 6344—
생성물1-Benzyl-4-(1-tert-butoxycarbonyl-piperidine-4-carbonyl)-[1,4]-diazepaneHCID 6035460389%

반응 단계

1-Benzyl-[1,4]-diazepane (3.78 g) and 1-tert-butoxycarbonyl-piperidine-4-carboxylic acid (5.0 g) were dissolved in DCM (150 ml) and TEA (3.6 ml) was added followed by HOBT (1.34 g) and finally EDC (4.90 g). The reaction was stirred at rt overnight. The reaction mixture was then evaporated to a minimum, re-dissolved in DCM (50 ml) and washed with saturated sodium hydrogen carbonate solution (3×50 ml) and brine (50 ml). The organic layer was dried (MgSO4) and evaporated to a crude which was purified by column chromatography [silica gel, step gradient 0-10% MeOH (containing 10% 0.880 ammonia solution) in DCM]. Fractions containing pure desired product were combined and evaporated to give the subtitled compound as a pale brown solid (7.1 g).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07592347B2
출처 데이터셋uspto-grants-2009_09
ORD IDord-32171a7d5ee746c5a0b602b6bdb50f56
출처 메모uspto-grants-2009_09