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(3-Methylpyridin-2-yl)methanamine → Pyrimidine-4-carboxamide, 26
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | (3-Methylpyridin-2-yl)methanamine | HCID 1514370 | — |
| 反応物 | 2-Amino-6-(2-furyl)pyrimidine-4-carboxylic acid | HCID 28799599 | — |
| 溶媒 | Dimethylformamide | HCID 6228 | — |
| 生成物 | Pyrimidine-4-carboxamide, 26 | HCID 11220580 | 35.2% |
反応手順
A suspension of 2-amino-6-(2-furyl)pyrimidine-4-carboxylic acid (206 mg, 1.0 mmol) in DMF (5 mL) was treated with N,N′-carbonyldiimidazole (162 mg, 1.0 mmol), stirred for 2 h, treated with 3-methylpyridine-2-methanamine (244 mg, 2.0 mmol), stirred for 2 h, poured onto water (50 mL) and extracted with EtOAc (2×25 mL). The extracts were washed with water, concentrated in vacuo, and the crude product was triturated with ether to give the title compound (109 mg, 35%) as a yellow solid.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US07875600B2 |
| 出典データセット | uspto-grants-2011_01 |
| ORD ID | ord-dfe8c1cc55d84b38ae4217bfa01c7d56 |
| 出典メモ | uspto-grants-2011_01 |