참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | N-methyl-2-pyrrolidone | HCID 13387 | — |
| 반응물 | 4-Aminotetrahydropyran | HCID 419223 | — |
| 반응물 | 2-(Methylsulfonyl)thieno[2,3-d]pyrimidine | HCID 21988356 | — |
| 용매 | Water | HCID 962 | — |
| 용매 | Ethyl Acetate | HCID 8857 | — |
| 생성물 | (Tetrahydropyran-4-yl)-thieno[2,3-d]pyrimidin-2-yl-amine | HCID 21988352 | 72.9% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US07091347B2 |
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| 출처 데이터셋 | uspto-grants-2006_08 |
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| ORD ID | ord-f0a73307f5ab435fad1e94b298214dad |
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| 출처 메모 | uspto-grants-2006_08 |
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