참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Potassium Carbonate | HCID 11430 | — |
| 반응물 | Ammonium Chloride | HCID 25517 | — |
| 반응물 | Phenol, 2,6-dichloro-4-fluoro- | HCID 94950 | — |
| 반응물 | 4-(2-Butynyloxy)-6-chloropyrimidine | HCID 12137602 | — |
| 용매 | Dimethylformamide | HCID 6228 | — |
| 생성물 | 4-(2-Butynyloxy)-6-(2,6-dichloro-4-fluorophenoxy)pyrimidine | HCID 22599825 | 61.4% |
반응 단계
To 2 ml of N,N-dimethylformamide were added 0.2 g of 4-chloro-6-(2-butynyloxy)pyrimidine, 0.23 g of potassium carbonate, and 0.20 g of 2,6-dichloro-4-fluorophenol, followed by stirring at 80° C. for 7 hours. The reaction mixture was then left for cooling to room temperature and poured into a saturated aqueous ammonium chloride solution, which was extracted three times with chloroform. The chloroform layers were combined, washed with diluted hydrochloric acid and then with water, and dried over anhydrous magnesium sulfate and then concentrated. The residue was subjected to silica gel column chromatography to give 0.22 g of 4-(2-butynyloxy)-6-(2,6-dichloro-4-fluorophenoxy)pyrimidine (the present compound (160)).
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US06838463B2 |
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| 출처 데이터셋 | uspto-grants-2005_01 |
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| ORD ID | ord-510097ca8d5b4f92b1b4b3e48fd49b98 |
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| 출처 메모 | uspto-grants-2005_01 |
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