HuagongsheHuagongshe Chemistry Print Report · For research reference only
HCID 135783976, compound → HCID 135783975, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | HCID 135783976 | HCID 135783976 | — |
| Reactant | HCID 178418361 | HCID 178418361 | — |
| Catalyst | Rhodium | HCID 23948 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 135783975 | HCID 135783975 | — |
Reaction Steps
16.2 G. of 1-ethyl-1,7-dihydro-4-(trifluoromethyl)-6H-pyrazolo[3,4-b]pyridin-6-one, dissolved in 250 ml. of absolute ethanol, are catalytically hydrogenated by means of rhodium on charcoal catalyst (5%) at a temperature of 90°-100°. The reaction is performed in an autoclave at a hydrogen pressure of 10 atm. for 14 hours. After cooling, the catalyst is filtered off and the solution evaporated to dryness. The residual 1-ethyl-1,4,5,7-tetrahydro-4-(trifluoromethyl)-6H-pyrazolo[3,4-b]pyridin-6-one is treated with hot hexane providing 13.3 g. (81.5%) of the compound, m.p. 129°-130°. Recrystallization from a mixture of benzene/petroleum ether (1:2) raises the melting point at 130°-132°.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US03935222 |
| Source dataset | uspto-grants-1976_01 |
| ORD ID | ord-13d2d399b4e642488f1d4865a2e40316 |
| Source note | uspto-grants-1976_01 |