HuagongsheHuagongshe Chemistry Print Report · For research reference only
(2-benzyloxy-7,8-dihydro-4H,6H-1,5,8a-triaza-azulen-5-yl)-(4-fluoro-phenyl)-methanone → HCID 178519626, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | (2-benzyloxy-7,8-dihydro-4H,6H-1,5,8a-triaza-azulen-5-yl)-(4-fluoro-phenyl)-methanone | HCID 86706495 | — |
| Catalyst | Palladium hydroxide | HCID 9942167 | — |
| Solvent | N,N-dimethylformamide ethyl acetate | HCID 22989253 | — |
| Product | HCID 178519626 | HCID 178519626 | 93% |
Reaction Steps
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.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09029366B2 |
| Source dataset | uspto-grants-2015_05 |
| ORD ID | ord-814ca853f9ba4a78a4b73d309bc5f3b8 |
| Source note | uspto-grants-2015_05 |