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HCID 57919756、化合物 → 2-[1-(cyclopropylmethyl)-5-oxo-1H-1,2,4-triazol-4(5H)-yl]-4-methylthiazole-5-carboxamide
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | HCID 57919756 | HCID 57919756 | — |
| 反応物 | 2-(1-(4-fluorobenzyl)-5-oxo-1H-1,2,4-triazol-4(5H)-yl)-4-methylthiazole-5-carboxylic acid | HCID 57919802 | — |
| 生成物 | 2-[1-(cyclopropylmethyl)-5-oxo-1H-1,2,4-triazol-4(5H)-yl]-4-methylthiazole-5-carboxamide | HCID 57919744 | 43% |
反応手順
Following the procedure as described in EXAMPLE 1, making variations as required to replace 2-(1-(4-fluorobenzyl)-5-oxo-1H-1,2,4-triazol-4(5H)-yl)-4-methylthiazole-5-carboxylic acid with 2-(1-(cyclopropylmethyl)-5-oxo-1H-1,2,4-triazol-4(5H)-yl)-4-methylthiazole-5-carboxylic acid, the title compound was obtained as an off-white solid in 43% yield: mp 180-181° C. (ethanol/water); 1H NMR (300 MHz, DMSO-d6) δ 8.73 (s, 1H), 7.63 (br, 2H), 3.66 (d, J=7.0 Hz, 2H), 2.55 (s, 3H), 1.21-1.11 (m, 1H), 0.54-0.48 (m, 2H), 0.38-0.32 (m, 2H); 13C NMR (75 MHz, DMSO-d6) δ 162.6, 151.3, 150.9, 149.5, 131.4, 122.9, 49.4, 16.8, 10.0, 3.3; MS (ES+) m/z 280.3 (M+1).
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US08318949B2 |
| 出典データセット | uspto-grants-2012_11 |
| ORD ID | ord-d1c92a3a52b64672bb84fa8e31a462d3 |
| 出典メモ | uspto-grants-2012_11 |