HuagongsheHuagongshe Chemistry Print Report · For research reference only
1H-Indole, 5-(phenylmethoxy)-1-(4-pyridinylmethyl)- → HCID 15292694, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 1H-Indole, 5-(phenylmethoxy)-1-(4-pyridinylmethyl)- | HCID 9904933 | — |
| Reactant | HCID 178418361 | HCID 178418361 | — |
| Catalyst | Palladium | HCID 23938 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 15292694 | HCID 15292694 | — |
Reaction Steps
To a suspension of 10% Pd/C (1.5 g) in 50 ml ethanol in a 500 ml Parr hydrogenation bottle, was added a suspension of 5-phenylmethoxy-1-(4-pyridinylmethyl)-1H-indole in 200 ml ethanol. The mixture was shaken at 50° C. under 50 psi hydrogen for one hour, then cooled, filtered, and the filtrate evaporated to a solid, 10 g, dec. 178° C. A sample of this material was eluted on a silica gel column with 2% methanol/dichloromethane via HPLC. The desired fractions were combined and evaporated to yield 2.3 g of 1-(4-pyridinylmethyl)-1H-indol-5-ol, as a solid, m.p. 185°-186° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05214058 |
| Source dataset | uspto-grants-1993_05 |
| ORD ID | ord-707089cba0b74e749188e78d81a62162 |
| Source note | uspto-grants-1993_05 |