참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Potassium Carbonate | HCID 11430 | — |
| 반응물 | Isopropylethylamine | HCID 88318 | — |
| 반응물 | 4-(2-Butynyloxy)-6-chloropyrimidine | HCID 12137602 | — |
| 용매 | Dimethylformamide | HCID 6228 | — |
| 생성물 | 4-(2-butynyloxy)-6-(N-ethyl-N-isopropylamino)pyrimidine | HCID 22599723 | 33.9% |
반응 단계
To 2 ml of N,N-dimethylformamide were added 183 mg of 4-chloro-6-(2-butynyloxy)pyrimidine, 166 mg of potassium carbonate, and 87 mg of N-ethylisopropylamine, followed by stirring at 60° C. for 7 hours. Then, 166 mg of potassium carbonate and 435 mg of N-ethylisopropylamine were added, and the mixture was stirred at 80° C. for 8 hours. Then, 166 mg of potassium carbonate and 435 mg of N-ethylisopropylamine were added, and the mixture was stirred at 120° C. for 5 hours. The reaction mixture was then left for cooling to room temperature and subjected to phase separation three times between ethyl acetate and an aqueous sodium chloride solution. The organic layer was dried over anhydrous magnesium sulfate and then concentrated. The residue was subjected to preparative silica gel thin layer chromatography to give 79 mg of 4-(2-butynyloxy)-6-(N-ethyl-N-isopropylamino)pyrimidine (the present compound (105)).
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US07291730B2 |
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| 출처 데이터셋 | uspto-grants-2007_11 |
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| ORD ID | ord-ca65dded8548451db2beda9fcb0e7236 |
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| 출처 메모 | uspto-grants-2007_11 |
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