HuagongsheHuagongshe Chemistry Print Report · For research reference only
Sodium borohydride → HCID 19357163, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Reactant | HCID 19357135 | HCID 19357135 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 19357163 | HCID 19357163 | 97% |
Reaction Steps
1-[N-(5-Acetyl-2-methoxy-6-methylpyridin-3-yl)-N-methylaminocarbonyl]-4-(3,5-dimethoxyphenyl)piperazine(0.47 mmol) was dissolved in anhydrous ethanol(15 ml) and thereto sodium borohydride(17.3 mg) was added, then followed by stirring at room temperature for 2 hrs. The resulting mixture was concentrated under the reduced pressure to remove ethanol and purified by column chromatography(ethylacetate:hexane=2:1) to obtain the titled compound.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06028195 |
| Source dataset | uspto-grants-2000_02 |
| ORD ID | ord-71e3c6defe0e4861b44781c9537b19b2 |
| Source note | uspto-grants-2000_02 |