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Ammonia → 6-Chloro-2-methylsulfanylpyrimidine-4-carboxamide
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | Ammonia | HCID 222 | — |
| 反応物 | Methyl 6-chloro-2-(methylsulfanyl)pyrimidine-4-carboxylate | HCID 238726 | — |
| 溶媒 | Chloroform | HCID 6212 | — |
| 生成物 | 6-Chloro-2-methylsulfanylpyrimidine-4-carboxamide | HCID 239276 | 103.4% |
反応手順
A 500 mL flask was charged with the 6-chloro-2-methylsulfanyl-pyrimidine-4-carboxylic acid methyl ester (4.37 g, 20 mmol), and chloroform (30 mL). Ammonia (57 mL, 7 M in methanol, 0.4 mol, 20 eq.) was added with stirring. HPLC analysis after 20 minutes indicated no starting methyl ester remained. The mixture was sparged with nitrogen for 30 min, then concentrated in vacuo, and dried under high vacuum to afford the 6-chloro-2-methylsulfanyl-pyrimidine-4-carboxylic acid amide (4.21 g, quant.) in sufficient purity for use in the next step. 1H NMR (500 MHz, CDCl3) □ 7.76 (s, 1H), 7.60 (br s, 1H), 5.97 (br s, 1H), 2.61 (s, 3H); ESI-MS m/z 204.1 (M+H)+.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US08822451B2 |
| 出典データセット | uspto-grants-2014_09 |
| ORD ID | ord-fbe7dfd91d8d45e19fc12674d442f8ad |
| 出典メモ | uspto-grants-2014_09 |