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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1393024생성일: 2026년 10월 27일

Triethylamine → Methyl-(2,3,11a-trimethyl-2,3,3a,4,5,5a,5b,6,8,9,10,11,11a,11b,12,13-hexadecahydro-1H-2-aza-pentaleno[1,6a-a]phenanthren-9-yl)-carbamic acid benzyl ester

https://huagongshe.com/reaction/1393024

반응식

참여 물질

역할이름HCID투입량
반응물TriethylamineHCID 8471—
반응물Benzyl chloroformateHCID 10387—
반응물KurchineHCID 551434—
용매DichloromethaneHCID 6344—
생성물Methyl-(2,3,11a-trimethyl-2,3,3a,4,5,5a,5b,6,8,9,10,11,11a,11b,12,13-hexadecahydro-1H-2-aza-pentaleno[1,6a-a]phenanthren-9-yl)-carbamic acid benzyl esterHCID 6742412166.2%

반응 단계

Compound 7B (20 mg, 0.058 mmol) and triethylamine (9.1 μL, 0.064 mmol) were dissolved in dichloromethane (1 mL). Benzyl chloroformate was added to it. The mixture was stirred at room temperature for 2 hours. The crude reaction mixture was purified on silica gel column using 0.5% ammonium hydroxide and 5% methanol in dichloromethane to give the desired product (18.4 mg, 66.2% yield).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07345034B2
출처 데이터셋uspto-grants-2008_03
ORD IDord-eb59f4586e3e4366be972476920c552d
출처 메모uspto-grants-2008_03