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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 892962생성일: 2026년 10월 25일

Sodium → Methyl (3S,E)-5-[4,5-bis(4-fluorophenyl)-2-(1-methylethyl)-1H-imidazol-1-yl]-3-hydroxy-4-pentenoate

https://huagongshe.com/reaction/892962

반응식

참여 물질

역할이름HCID투입량
반응물SodiumHCID 5360545—
반응물(S)-1-hydroxy-1,1,2-triphenyleth-2-yl (3S,E)-5-[4,5-bis(4-fluorophenyl)-2-(1-methylethyl)-1H-imidazol-1-yl]-3-hydroxy-4-pentenoateHCID 14849798—
용매MethanolHCID 887—
생성물Methyl (3S,E)-5-[4,5-bis(4-fluorophenyl)-2-(1-methylethyl)-1H-imidazol-1-yl]-3-hydroxy-4-pentenoateHCID 1484980082%

반응 단계

A stirred suspension of (S)-1-hydroxy-1,1,2-triphenyleth-2-yl (3S,E)-5-[4,5-bis(4-fluorophenyl)-2-(1-methylethyl)-1H-imidazol-1-yl]-3-hydroxy-4-pentenoate (3.11 g) in methanol (30 ml) was treated with a solution of sodium (110 mg) in methanol (20 ml) plus methanol washings (2×5 ml). The resulting orange solution was stirred at room temperature for 2.5 h then the reaction mixture was concentrate. This was dissolved in dichloromethane (150 ml) and the solution was washed with water (50 ml) and brine (2×50 ml). The combined washings were extracted with dichloromethane (50 ml) and the combined organic phases were dried and evaporated to a pale buff solid (3.13 g). This was purified by CC eluting with System A 1:1 to give the title compound (1.588 g) as a white crystalline solid, νmax (nujol) 1738 cm-1 (C=O).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05120848
출처 데이터셋uspto-grants-1992_06
ORD IDord-40d4fd87b891429f97138470c0771931
출처 메모uspto-grants-1992_06