関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | Thiobenzamide | HCID 683563 | — |
| 反応物 | 2-Bromo-1-(2-phenylpyrimidin-5-yl)ethanone | HCID 59252454 | — |
| 溶媒 | Ethanol | HCID 702 | — |
| 生成物 | 2-Phenyl-4-(2-phenylpyrimidin-5-yl)thiazole | HCID 59252447 | 46% |
反応手順
A mixture consisting of 2-bromo-1-(2-phenylpyrimidin-5-yl)ethanone (Example 14, Step B, 50 mg, 0.18 mmol), thiobenzamide (TCl America, 25 mg, 0.18 mmol) and absolute ethanol (4 mL) in a capped scintillation vial was heated to near boiling for several minutes and was subsequently allowed to cool to room temperature. A white solid precipitated within minutes. The precipitate was collected by vacuum filtration. Light ethanol rinse, suction, and drying under high vacuum at room temperature afforded the title compound (26 mg, 46% yield) as an off-white solid; melting point 214.4-216.1° C.; 1H-NMR (400 MHz; DMSO-d6) δ 9.54 (s, 2H), 8.54 (s, 1H), 8.47 (m, 2H), 8.08 (m, 2H), 7.62-7.54 (m, 6H); LC/MS (ESI+) m/z 316.1, (ESI−) m/z 337.2 (M−1+Na+); H-PGDS FPBA IC50: >20 μM.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| 特許番号 | US08536185B2 |
|---|
| 出典データセット | uspto-grants-2013_09 |
|---|
| ORD ID | ord-59b63460ac33409aa614d4fadb29ae68 |
|---|
| 出典メモ | uspto-grants-2013_09 |
|---|