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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 430704생성일: 2026년 10월 25일

Imidazole → 3-Tert-butyldimethylsilyloxy-17-cyclopropylmethyl-4,5alpha-epoxy-14beta-hydroxy-6-oxomorphinan

https://huagongshe.com/reaction/430704

반응식

참여 물질

역할이름HCID투입량
반응물ImidazoleHCID 795—
반응물WaterHCID 962—
반응물tert-Butyldimethylsilyl chlorideHCID 28928—
반응물Naltrexone HydrochlorideHCID 5485201—
용매Diethyl EtherHCID 3283—
생성물3-Tert-butyldimethylsilyloxy-17-cyclopropylmethyl-4,5alpha-epoxy-14beta-hydroxy-6-oxomorphinanHCID 1439477976%

반응 단계

3.49 g of naltrexone hydrochloride was suspended in 10.5 ml of N,N-dimethylfonnamde. After adding 3.46 g of imidazole, 3.48 g of tert-butyldimethylchlorosilane was added followed by stirring for 35 minutes at room temperature. 30 ml of water and 50 ml of diethyl ether were added to the reaction system followed by separation. The aqueous layer was extracted twice with 30 ml of diethyl ether. The combined extracts were dried over anhydrous sodium sulfate and concentrated. The resulting residue was recrystallized from ethanol to obtain 3.2 g of the target compound (yield: 76%).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06323212B1
출처 데이터셋uspto-grants-2001_11
ORD IDord-729b126d6f8d4bf79da0b2f86e57e8d0
출처 메모uspto-grants-2001_11