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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1352772생성일: 2026년 10월 26일

Triethylamine → 4-Benzylthio-5-methoxycarbonyl-6-(4-hydroxypiperidin-1-yl)-2-(5,6,7,8-tetrahydroimidazo[1,2-a]pyrazin-7-yl)pyrimidine

https://huagongshe.com/reaction/1352772

반응식

참여 물질

역할이름HCID투입량
반응물TriethylamineHCID 8471—
반응물DimethylacetamideHCID 31374—
반응물5,6,7,8-Tetrahydroimidazo(1,2-a)pyrazineHCID 13247046—
반응물4-Benzylthio-5-methoxycarbonyl-6-(4-hydroxypiperidine-1-yl)-2-chloropyrimidineHCID 17848266—
용매Citric AcidHCID 311—
생성물4-Benzylthio-5-methoxycarbonyl-6-(4-hydroxypiperidin-1-yl)-2-(5,6,7,8-tetrahydroimidazo[1,2-a]pyrazin-7-yl)pyrimidineHCID 17848277—

반응 조건

온도10 °C

반응 단계

A mixture of 4-benzylthio-5-methoxycarbonyl-6-(4-hydroxypiperidine-1-yl)-2-chloropyrimidine (prepared in the above (4)) 120 mg, 5,6,7,8-tetrahydroimidazo[1,2-a]pyrazine 70 mg, triethylamine 57 mg and N,N-dimethylacetamide 3 ml is stirred at 10° C. for 3 hours. The reaction mixture is diluted with an aqueous citric acid solution and extracted with ethyl acetate. The water layer is made basic with an aqueous sodium hydrogen carbonate solution and extracted with ethyl acetate. The organic layer is washed, dried and concentrated in vacuo to give 4-benzylthio-5-methoxycarbonyl-6-(4-hydroxypiperidin-1-yl)-2-(5,6,7,8-tetrahydroimidazo[1,2-a]pyrazin-7-yl)pyrimidine as a colorless foam, 105 mg.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07220736B2
출처 데이터셋uspto-grants-2007_05
ORD IDord-bb393e312ca14d8d9c4dd486fe86417e
출처 메모uspto-grants-2007_05