HuagongsheHuagongshe Chemistry Print Report · For research reference only
Chloroform → 2-amino-N-[(1-diphenylmethylpiperidin-4-yl)methyl]benzamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Chloroform | HCID 6212 | — |
| Reactant | Isatoic Anhydride | HCID 8359 | — |
| Reactant | 4-Aminomethyl-1-diphenylmethylpiperidine | HCID 53786046 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 2-amino-N-[(1-diphenylmethylpiperidin-4-yl)methyl]benzamide | HCID 67594819 | — |
Reaction Steps
A solution of 4-aminomethyl-1-diphenylmethylpiperidine (2.5 g, 9.15 mmol) in dichloromethane (10 ml) was added to a suspension of isatoic anhydride (1.0 g, 6.1 mmol) in dichloromethane (25 ml) at room temperature. The reaction mixture was stirred for 1 hour and then poured into chloroform and washed with 5% NaHCO3 solution. The organic layer was concentrated. The residue was dissolved in dichloromethane (25 ml) and poured into hexane (400 ml) to give 2-amino-N-[(1-diphenylmethylpiperidin-4-yl)methyl]benzamide as precipitate (100%): mp 153°-154° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05872115 |
| Source dataset | uspto-grants-1999_02 |
| ORD ID | ord-21eed670ff024463a2b3dfb82b4f5f51 |
| Source note | uspto-grants-1999_02 |