돌아가기
Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 481687생성일: 2026년 10월 25일

(2s)-Glycidyl indol-4-yl ether → (2S)-(+)-3-[4-(5-fluoro-3-indolyl)piperidin-1-yl]-1-(4-indolyloxy)-2-propanol

https://huagongshe.com/reaction/481687

반응식

참여 물질

역할이름HCID투입량
반응물(2s)-Glycidyl indol-4-yl etherHCID 10943254—
반응물5-fluoro-3-(piperidin-4-yl)-1H-indoleHCID 11769929—
용매Dimethyl sulfoxide methanolHCID 22036561—
생성물(2S)-(+)-3-[4-(5-fluoro-3-indolyl)piperidin-1-yl]-1-(4-indolyloxy)-2-propanolHCID 70216375—

반응 단계

The title compound was prepared in a fashion similar to that described in Example 193 from 5-fluoro-3-(piperidin-4-yl)-1H-indole (0.87 g, 4.0 mmol) and (S)-(+)-4-(oxiranylmethoxy)-1H-indole (0.76 g, 4.0 mmol). The product was isolated as a white foam. Yield 1.14 g (70%). mp 94°-97° C. FDMS m/e=407 (M+ of free base). α[D]589 =+8.36 (c=1.00, methanol/dimethylsulfoxide).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05789402
출처 데이터셋uspto-grants-1998_08
ORD IDord-10863575a0dc473ea1663217adddb876
출처 메모uspto-grants-1998_08