関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | Phosphorus trichloride | HCID 24387 | — |
| 反応物 | 2-Chloro-3-pyridylamine | HCID 80528 | — |
| 反応物 | 3-Acetamidothiophene-2-carboxylic acid | HCID 2807579 | — |
| 溶媒 | Pyridine | HCID 1049 | — |
| 生成物 | 2-methyl-3-(2-chloropyrid-3-yl)-3H-thieno[3,2-d]pyrimidin-4-one | HCID 18350679 | 63% |
反応手順
To a mixture of pyridine (4 mL), 3-amino-2-chloropyridine (0.514 g, 4 mmol), and 3-acetamidothiophene-2-carboxylic acid (0.370 g, 4 mmol) was added phosphorus trichloride (0.02 mL, 2.3 mmol). The reaction was heated to 105° C. for 3 hours, cooled to ambient temperature and partitioned between ethyl acetate and water. Phases were separated and the aqueous layer was extracted with ethyl acetate. The combined organic phase was washed with water and brine, dried over sodium sulfate and concentrated to a greenish brown oil. This residue was flash chromatographed on silica gel (20×120 mm) eluting with 20-40% ethyl acetate/hexane to afford 0.350 g (63%) of 2-methyl-3-(2-chloropyrid-3-yl)-3H-thieno[3,2-d]pyrimidin-4-one as a yellow foam.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US05962457 |
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| 出典データセット | uspto-grants-1999_10 |
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| ORD ID | ord-a19d1dcd5bd84cda949f2aa82c95c1ae |
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| 出典メモ | uspto-grants-1999_10 |
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