関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | Acetonitrile | HCID 6342 | — |
| 反応物 | Phosphorus oxychloride | HCID 24813 | — |
| 反応物 | 2-(4-Chlorophenyl)-6-hydroxypyrimidine-4-carboxylic acid | HCID 135878882 | — |
| 溶媒 | Water | HCID 962 | — |
| 生成物 | 6-Amino-2-(4-chlorophenyl)pyrimidine-4-carboxylic acid | HCID 46863985 | — |
反応手順
To phosphorus oxychloride (180 mL) was added 2-(4-chlorophenyl)-1,6-dihydro-6-oxo-4-pyrimidinecarboxylic acid (i.e. the product of Step A) (81.81 g, 326 mmol). The mixture was heated to 90° C. for 2.5 h. After cooling to room temperature the reaction mixture was slowly added to 1:2 acetonitrile:water (1.5 L) while keeping the temperature between 35 and 45° C. After the reaction mixture was stirred at room temperature for 30 minutes the resulting solid was isolated by filtration and washed with water. The solid was then combined with aqueous ammonia (5%, 2.1 L) and heated to 80° C. for 18 h. After 2 days at room temperature the solid was isolated by filtration and washed with water. A second crop was obtained by cooling the filtrate and refiltering. The combined solids were dried to afford the title compound (58.8 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-1098f0148d4746dd829304c89117beb2 |
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| 出典メモ | uspto-grants-2011_01 |
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