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HRID 440117作成日:2026年10月25日

Ethylmorpholine → Ro 31-8875

https://huagongshe.com/reaction/440117

反応式

関与物質

役割名称HCID仕込み量
反応物EthylmorpholineHCID 7525—
反応物DicyclohexylcarbodiimideHCID 10868—
反応物Benzyloxycarbonyl-asparagineHCID 75314—
反応物(3S,4aS,8aS)-2-((2R,3S)-3-amino-2-hydroxy-4-phenylbutyl)-N-tert-butyldecahydroisoquinoline-3-carboxamideHCID 9865804—
反応物HCID 178418300HCID 178418300—
溶媒TetrahydrofuranHCID 8028—
溶媒Ethyl AcetateHCID 8857—
生成物Ro 31-8875HCID 45368047.8%

反応手順

A solution of 561 mg of 2-[3(S)-amino-2(R)-hydroxy-4-phenylbutyl]-N-tert.butyl-decahydro-(4aS,8aS)-isoquinoline-3(S)-carboxamide and 372 mg of N-(benzyloxycarbonyl)-L-asparagine in 20 ml of dry tetrahydrofuran was cooled in an ice/salt mixture. 189 mg of hydroxybenzotriazole, 161 mg of N-ethylmorpholine and 317 mg of dicyclohexylcarbodiimide were added and the mixture was stirred for 16 hours. The mixture was then diluted with ethyl acetate and filtered. The filtrate was washed with aqueous sodium bicarbonate solution and sodium chloride solution. The solvent was removed by evaporation and the residue was chromatographed on silica gel using dichloromethane/methanol (9:1) for the elution to give 434 mg of 2-[3(S)-[[N-(benzyloxycarbonyl)-L-asparaginyl]amino]-2(R)-hydroxy-4-phenylbutyl]-N-tert.butyl-decahydro-(4aS,8aS )-isoquinoline-3(S)-carboxamide as a white solid from methanol/diethyl ether: MS: m/e 650 [M+H]+.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05516913
出典データセットuspto-grants-1996_05
ORD IDord-b6ff8e7fff56415d9f12c21f47e74e2f
出典メモuspto-grants-1996_05