돌아가기
Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 433140생성일: 2026년 10월 25일

6-fluoro-3-(1,2,3,6-tetrahydropyridin-4-yl)-1H-indole → HCID 12114960, 화합물

https://huagongshe.com/reaction/433140

반응식

참여 물질

역할이름HCID투입량
반응물6-fluoro-3-(1,2,3,6-tetrahydropyridin-4-yl)-1H-indoleHCID 11053072—
반응물[(2R)-8-methoxy-3,4-dihydro-2H-chromen-2-yl]methyl 4-methylbenzenesulfonateHCID 12114957—
용매Dimethyl SulfoxideHCID 679—
용매Ethyl AcetateHCID 8857—
생성물HCID 12114960HCID 1211496062%

반응 조건

온도80 °C

반응 단계

To a solution of [(2R)-8-methoxy-3,4-dihydro-2H-chromen-2-yl]methyl 4-methylbenzenesulfonate (0.348 g, 1.00 mmol) in methyl sulfoxide (20 mL) was added 6-fluoro-3-(1,2,3,6-tetrahydro-4-pyridinyl)-1H-indole (0.865 g, 4.00 mmol) and the reaction mixture was heated to 80° C. for 12 h. The reaction mixture was allowed to cool to room temperature and was diluted with ethyl acetate (200 mL), washed with water (2×100 mL), aqueous sodium chloride (100 mL), dried (magnesium sulfate) and the solvent was removed in vacuo to give a crude solid. Purification by flash column chromatography (silica, ethyl acetate:hexanes 4:1) followed by recrystallization from ethanol provided 0.243 g (62%, 40% ee) of 6-fluoro-3-(1-{[(2R)-8-methoxy-3,4-dihydro-2H-chromen-2-yl]methyl}-1,2,3,6-tetrahydro-4-pyridinyl)-1H-indole as a tan crystalline powder. [α]D25=−27.14 (c 9.95 in chloroform, 40% ee); Rf=0.47 (silica, ethyl acetate:hexanes 4:1); mp >170° C. dec; Anal. Calcd. for C24H25FN2O2.0.1 H2O: C, 73.11; H, 6.44; N, 7.11. Found: C, 72.81; H, 6.36; N, 7.06.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06667322B2
출처 데이터셋uspto-grants-2003_12
ORD IDord-3a11cad4e0a44ce7b04de8a9106a5c1f
출처 메모uspto-grants-2003_12