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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 9771생성일: 2026년 10월 23일

N-methyl-2-pyrrolidone → (Tetrahydropyran-4-yl)-thieno[2,3-d]pyrimidin-2-yl-amine

https://huagongshe.com/ko/reaction/9771

반응식

참여 물질

역할이름HCID투입량
반응물N-methyl-2-pyrrolidoneHCID 13387—
반응물4-AminotetrahydropyranHCID 419223—
반응물2-(Methylsulfonyl)thieno[2,3-d]pyrimidineHCID 21988356—
용매WaterHCID 962—
용매Ethyl AcetateHCID 8857—
생성물(Tetrahydropyran-4-yl)-thieno[2,3-d]pyrimidin-2-yl-amineHCID 2198835272.9%

반응 조건

온도100 °C

반응 단계

A mixture of 2-methanesulfonyl-thieno[2,3-d]pyrimidine (1.58 g, 7.37 mmol), 4-aminotetrahydropyran (2.24 g, 3 eq) and 1-methyl-2-pyrolidinone (2 mL) was heated to 100° C. with stirring for about 7 hours and continued heating at 80° C. overnight. The reaction mixture was cooled to room temperature and diluted with ethyl acetate (180 mL)/water (60 mL). The layers were separated, and the organic layer was washed successively with water (4×60 mL) and brine (1×60 mL). The organic layer was then dried over magnesium sulfate, filtered and concentrated to give 1.7 g of the crude product. Purification by column chromatography on silica gel eluting with 25% ethyl acetate in hexanes afforded the title compound as a white powder (1.264 g) ((M+H)+=236, M.P.=127.0–130.0° C.).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07091347B2
출처 데이터셋uspto-grants-2006_08
ORD IDord-f0a73307f5ab435fad1e94b298214dad
출처 메모uspto-grants-2006_08