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HRID 651048作成日:2026年10月26日

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

https://huagongshe.com/reaction/651048

反応式

関与物質

役割名称HCID仕込み量
反応物ImidazoleHCID 795—
反応物WaterHCID 962—
反応物tert-Butyldimethylsilyl chlorideHCID 28928—
反応物Naltrexone HydrochlorideHCID 5485201—
溶媒Diethyl EtherHCID 3283—
溶媒DimethylformamideHCID 6228—
生成物3-Tert-butyldimethylsilyloxy-17-cyclopropylmethyl-4,5alpha-epoxy-14beta-hydroxy-6-oxomorphinanHCID 1439477976%

反応手順

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%).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06277859B1
出典データセットuspto-grants-2001_08
ORD IDord-4149595f1c744e1abe8cce13f2e70210
出典メモuspto-grants-2001_08