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Methylamine → 2-chloro-N-methyl-5-nitropyrimidin-4-amine
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | Methylamine | HCID 6329 | — |
| 反応物 | Diisopropylethylamine | HCID 81531 | — |
| 反応物 | 2,4-Dichloro-5-nitropyrimidine | HCID 521266 | — |
| 溶媒 | Tetrahydrofuran | HCID 8028 | — |
| 溶媒 | Ethyl Acetate | HCID 8857 | — |
| 生成物 | 2-chloro-N-methyl-5-nitropyrimidin-4-amine | HCID 7147232 | 100% |
反応手順
To a solution of 2,4-dichloro-5-nitropyrimidine (5 g, 26 mmol) in THF (50 mL) was added diisopropylethylamine (3.36 g, 26 mmol) at −78° C., followed by the dropwise addition of methylamine (13 mL, 2 mol/L in methanol, 26 mmol). After the addition, the mixture was warmed to RT and stirred for 3 h. The reaction mixture was then diluted with ethyl acetate and washed with brine (50 mL*3). The organic layer was dried over sodium sulfate, filtered and concentrated to give the title compound (4.4 g, 100%) as a yellow solid. MS (ES+) C5H5ClN4O2 requires: 188, 190. found: 189, 191 [M+H]+.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US09340514B2 |
| 出典データセット | uspto-grants-2016_05 |
| ORD ID | ord-0743059575294e81abd40c482cef0bd1 |
| 出典メモ | uspto-grants-2016_05 |