HuagongsheHuagongshe Chemistry Print Report · For research reference only
1-(3-Fluoro-4-pyridinylamino)-5-phenylmethoxy-1H-indole → 1-(3-Fluoro-4-pyridinylamino)-1H-indol-5-ol
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 1-(3-Fluoro-4-pyridinylamino)-5-phenylmethoxy-1H-indole | HCID 19900464 | — |
| Reactant | HCID 178418361 | HCID 178418361 | — |
| Catalyst | Palladium | HCID 23938 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | 1-(3-Fluoro-4-pyridinylamino)-1H-indol-5-ol | HCID 19900485 | 137.1% |
Reaction Steps
In a 500 ml Parr hydrogenation bottle, 10% Pd/C (1.0 g) was suspended in 50 ml ethanol, and to this was added a solution of 1-(3-fluoro-4-pyridinylamino)-5-phenylmethoxy-1H-indole (5.0 g) in 200 ml ethanol. The mixture was shaken at 50° C. under 50 psi hydrogen gas for two hours. After cooling, the mixture was filtered, and the filtrate was concentrated to give an oil (5.0 g) which was eluted on a silica gel column with ethyl acetate/dichloromethane (1:1) via HPLC. The desired fractions were combined and concentrated to give a crystalline solid, 3.5 g, m.p. 70°-73° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05102891 |
| Source dataset | uspto-grants-1992_04 |
| ORD ID | ord-21665ff9206c436493bf5880b3acc1c8 |
| Source note | uspto-grants-1992_04 |