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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 651717생성일: 2026년 10월 27일

Ammonia → Sumatriptan

https://huagongshe.com/reaction/651717

반응식

참여 물질

역할이름HCID투입량
반응물AmmoniaHCID 222—
반응물Ammonium ChlorideHCID 25517—
반응물CalciumHCID 5460341—
반응물1-[1-benzyl-3-[2-(dimethylamino)ethyl]-1H-indol-5-yl]-N-diphenylmethyl-N-methylmethanesulfonamideHCID 21709116—
용매WaterHCID 962—
용매TetrahydrofuranHCID 8028—
생성물SumatriptanHCID 535856.4%

반응 단계

To a stirred slurry of calcium turnings (243 mg, 6 mmol) in tetrahydrofuran (4 ml) at −40° C. was condensed liquid ammonia (4 ml). The blue bronze was stirred at −50 to −40° C. for a further 15 min, before a solution of 1-[1-benzyl-3-[2-(dimethylamino)ethyl]-1H-indol-5-yl]-N-diphenylmethyl-N-methylmethanesulfonamide (from step (e), 836 mg, 1.5 mmol) in tetrahydrofuran (2 ml) was added dropwise, maintaining the temperature below −40° C. The dark blue solution was stirred at −40° C. for a further 30 minutes, before saturated ammonium chloride solution (10 ml) was added dropwise and the grey solution warmed to ambient temperature. Water (10 ml) was then added and the white slurry stirred for 15 min, before being filtered in vacuo. The solid was then dissolved in 5N HCl (12 ml) and the resulting orange solution extracted with ethyl acetate (10 ml). The pH of the aqueous phase was then adjusted (pH=10) with 10N NaOH which resulted in precipitation. The solid was filtered and dried in vacuo at 50° C. overnight to yield the title compound (250 mg, 56%) as a white solid. m.p. 159-163° C.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06281357B1
출처 데이터셋uspto-grants-2001_08
ORD IDord-a8115c07969840e4816a657bb1e7c9bf
출처 메모uspto-grants-2001_08