HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ammonium Chloride → N-[4-(1-hydroxyethyl)phenyl]-3-(piperidin-1-ylsulfonyl)benzamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ammonium Chloride | HCID 25517 | — |
| Reactant | N-(4-acetylphenyl)-3-(piperidin-1-ylsulfonyl)benzamide | HCID 1127074 | — |
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | N-[4-(1-hydroxyethyl)phenyl]-3-(piperidin-1-ylsulfonyl)benzamide | HCID 66871890 | 98.5% |
Reaction Steps
Sodium borohydride (8.8 mg) was added to an ethanol (2.0 mL) solution of the compound (30.0 mg) obtained in Example 92, and stirred overnight at room temperature. Aqueous saturated ammonium chloride solution was added to the reaction liquid, extracted three times with ethyl acetate, and dried with sodium sulfate. The drying agent was removed through filtration, and the solvent was evaporated off under reduced pressure. The residue was purified through silica gel column chromatography (ethyl acetate/hexane=from 0% to 80%, gradient) to give the entitled compound (29.7 mg, 98%) as a white solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08420823B2 |
| Source dataset | uspto-grants-2013_04 |
| ORD ID | ord-0e07175189e54c739a0577b72fc52c54 |
| Source note | uspto-grants-2013_04 |