HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1597313Generated: October 29, 2026
HCID 10679101, compound → HCID 15463736, compound
https://huagongshe.com/reaction/1597313
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | HCID 10679101 | HCID 10679101 | — |
| Reactant | HCID 10937790 | HCID 10937790 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 15463736 | HCID 15463736 | 81% |
Reaction Steps
To a solution of chloromethyl N-phenylcarbamate (220 mg), which is prepared by the method disclosed in Synth. Commun., 1996, 26, 4253, in ethanol (20 ml) is added dropwise a solution of 4-amino-5-chloro-2-methoxy-N-[1-(4-piperidinylmethyl)-4-piperidinyl]benzamide (910 mg) in ethanol (10 ml) at room temperature, and the mixture is stirred at room temperature for 7 hours. The mixture is concentrated to dryness under reduced pressure, and the residue is dissolved in chloroform, washed with water and a saturated aqueous sodium chloride solution, dried over anhydrous magnesium sulfate, and the solvent is evaporated under reduced pressure. The residue is purified by silica gel column chromatography (eluent; chloroform:methanol=30:1) to give the desired compound (480 mg) as white amorphous.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US06294555B1 |
|---|
| Source dataset | uspto-grants-2001_09 |
|---|
| ORD ID | ord-a11a04276dde4e81b34d5cc7ee7a253b |
|---|
| Source note | uspto-grants-2001_09 |
|---|