関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | Water | HCID 962 | — |
| 反応物 | Chlorosuccinimide | HCID 31398 | — |
| 反応物 | 6-Amino-2-(4-chlorophenyl)pyrimidine-4-carboxylic acid | HCID 46863985 | — |
| 溶媒 | Dimethylformamide | HCID 6228 | — |
| 生成物 | 6-Amino-5-chloro-2-(4-chlorophenyl)pyrimidine-4-carboxylic acid | HCID 46863984 | — |
反応手順
To a solution of 6-amino-2-(4-chlorophenyl)-4-pyrimidinecarboxylic acid (i.e. the product of Step B) (75 g, 300 mmol) in N,N-dimethylformamide (300 mL) at 50° C. was added portionwise N-chlorosuccinimide (44.1 g, 330 mmol). The temperature of the reaction mixture increased exothermically to 65° C. Then the reaction mixture was heated at 55° C. for 3 h. Additional N-chlorosuccinimide (14 g, 90 mmol) was added portionwise, and the reaction mixture was maintained at 55° C. for 30 minutes. After the reaction mixture was cooled water was added. The resulting solid was isolated by filtration, washed with water, dissolved in ethyl acetate, washed with water and dried. The solvent was removed using a rotary evaporator to afford the title product, a compound of the present invention, as a tan solid (73.68 g).
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US07863220B2 |
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| 出典データセット | uspto-grants-2011_01 |
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| ORD ID | ord-8771eef4f9134e969b606860399eab85 |
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| 出典メモ | uspto-grants-2011_01 |
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