関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | Potassium Carbonate | HCID 11430 | — |
| 反応物 | Ammonium Chloride | HCID 25517 | — |
| 反応物 | Phenol, 2,6-dichloro-4-fluoro- | HCID 94950 | — |
| 反応物 | 4-(2-Butynyloxy)-6-chloropyrimidine | HCID 12137602 | — |
| 溶媒 | Dimethylformamide | HCID 6228 | — |
| 生成物 | 4-(2-Butynyloxy)-6-(2,6-dichloro-4-fluorophenoxy)pyrimidine | HCID 22599825 | 61.4% |
反応手順
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)).
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US07291730B2 |
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| 出典データセット | uspto-grants-2007_11 |
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| ORD ID | ord-c47668dd6bc14b65bc4e28ebedbff020 |
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| 出典メモ | uspto-grants-2007_11 |
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