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HRID 651048생성일: 2026년 10월 26일

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

https://huagongshe.com/reaction/651048

반응식

참여 물질

역할이름HCID투입량
반응물ImidazoleHCID 795—
반응물WaterHCID 962—
반응물tert-Butyldimethylsilyl chlorideHCID 28928—
반응물Naltrexone HydrochlorideHCID 5485201—
용매Diethyl EtherHCID 3283—
용매DimethylformamideHCID 6228—
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-dimethylformamide. 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 번호US06277859B1
출처 데이터셋uspto-grants-2001_08
ORD IDord-4149595f1c744e1abe8cce13f2e70210
출처 메모uspto-grants-2001_08