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m-Toluidine → Methyl 2-chloro-4-methyl-6-(m-tolylamino)pyrimidine-5-carboxylate
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | m-Toluidine | HCID 7934 | — |
| 反応物 | Diisopropylethylamine | HCID 81531 | — |
| 反応物 | Methyl 2,4-dichloro-6-methylpyrimidine-5-carboxylate | HCID 57531614 | — |
| 溶媒 | Acetonitrile | HCID 6342 | — |
| 溶媒 | Ethyl Acetate | HCID 8857 | — |
| 生成物 | Methyl 2-chloro-4-methyl-6-(m-tolylamino)pyrimidine-5-carboxylate | HCID 58317549 | 97% |
反応手順
A mixture of methyl 2,4-dichloro-6-methylpyrimidine-5-carboxylate (940 mg, 4.25 mmol), m-toluidine (0.461 mL, 4.25 mmol) and N-ethyldiisopropylamine (1.481 mL, 8.51 mmol) in CH3CN (30 mL) was heated under reflux for 3 h. The mixture was diluted with EtOAc, and was washed with brine and water. The organic extract was dried and concentrated under reduced pressure to give the title compound as a light yellow solid (1.2 g, 97%). [M+H] calc'd for C14H14N3ClO2, 292; found, 292.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US09108970B2 |
| 出典データセット | uspto-grants-2015_08 |
| ORD ID | ord-5a1eb3af0b1443d4b20b1064e6aa8b43 |
| 出典メモ | uspto-grants-2015_08 |