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(2-benzyloxy-7,8-dihydro-4H,6H-1,5,8a-triaza-azulen-5-yl)-(4-fluoro-phenyl)-methanone → HCID 178519626、化合物
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | (2-benzyloxy-7,8-dihydro-4H,6H-1,5,8a-triaza-azulen-5-yl)-(4-fluoro-phenyl)-methanone | HCID 86706495 | — |
| 触媒 | Palladium hydroxide | HCID 9942167 | — |
| 溶媒 | N,N-dimethylformamide ethyl acetate | HCID 22989253 | — |
| 生成物 | HCID 178519626 | HCID 178519626 | 93% |
反応手順
A solution of (2-benzyloxy-7,8-dihydro-4H,6H-1,5,8a-triaza-azulen-5-yl)-(4-fluoro-phenyl)-methanone (0.902 g, 2.47 mmol) in a mixture of AcOEt/DMF (25/25 mL) was hydrogenated in a H-Cube reactor (1.5 ml/min, 70 mm, Pd(OH)2/C cartridge, full H2 mode, 80° C., 1 cycle). The solvents were evaporated in vacuo to yield (4-Fluoro-phenyl)-(2-hydroxy-7,8-dihydro-4H,6H-1,5,8a-triaza-azulen-5-yl)-methanone (0.63 g, 93% yield) as a colorless oil, that was used in the next step without further purification.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US09029366B2 |
| 出典データセット | uspto-grants-2015_05 |
| ORD ID | ord-814ca853f9ba4a78a4b73d309bc5f3b8 |
| 出典メモ | uspto-grants-2015_05 |