HuagongsheHuagongshe Chemistry Print Report · For research reference only
Sodium borohydride → 1-(4-Ethylpiperazin-1-yl)-3-(2-hydroxy-2-phenylethyl)isoquinoline
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Reactant | 1-(4-Ethylpiperazin-1-yl)-3-phenacylisoquinoline | HCID 22503451 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | 1-(4-Ethylpiperazin-1-yl)-3-(2-hydroxy-2-phenylethyl)isoquinoline | HCID 22503272 | 87.6% |
Reaction Steps
To a solution of the resulting 1-(4-ethylpiperazin-1-yl)-3-phenacylisoquinoline (0.92 g) in methanol (30 ml) was added sodium borohydride (0.12 g) at room temperature. One hr later, the reaction mixture was concentrated. The resulting residue was partitioned between ethyl acetate and water, and extracted with ethyl acetate. The resulting organic layer was washed with water and brine, and dried over magnesium sulfate. The solvent was removed, to give the title compound (0.81 g) as a pale yellow oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06790844B2 |
| Source dataset | uspto-grants-2004_09 |
| ORD ID | ord-2fce232d95244732afc1c19f98d8e4bd |
| Source note | uspto-grants-2004_09 |