참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Ammonia | HCID 222 | — |
| 반응물 | Sulfolane | HCID 31347 | — |
| 반응물 | 2-Chloro-5-methylaniline | HCID 66770 | — |
| 반응물 | 4,6-Dichloropyrimidine | HCID 70943 | — |
| 용매 | Dichloromethane | HCID 6344 | — |
| 생성물 | 4-Chloro-6-(2-chloro-5-methylanilino)pyrimidine | HCID 18009138 | 57.4% |
반응 단계
Tetramethylene sulphone (10 ml) was added to 4,6-dichloropyrimidine (25.0 g, 170 mmol) and heated to 125° C. 2-Chloro-5-methylaniline (11.90 g, 84 mmol) was added portion wise over 20 mins. The reaction mixture was heated at 125° C. for 2 hours. The reaction was allowed to cool to room temperature and DCM (200 ml) was added. The mixture was basified to pH 9-10 with methanolic ammonia and evaporated onto silica (15 g). The residue was purified by column chromatography eluting with EtOAc:isohexane (10:90) to give a white solid (12.25 g, 29%). NMR (300 MHz): 2.3 (s, 3H), 6.7 (s, 1H), 7.0 (d, 1H), 7.4 (d, 1H), 7.5 (s, 1H), 8.4 (s, 1H), 9.4 (s, 1H); m/z 254 (MH+).
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US06632820B1 |
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| 출처 데이터셋 | uspto-grants-2003_10 |
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| ORD ID | ord-a791a57bdae54dddbdc61f321eca5112 |
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| 출처 메모 | uspto-grants-2003_10 |
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