HuagongsheHuagongshe Chemistry Print Report · For research reference only
O-Toluidine → 4-[(6,11-Dihydro-5H-dibenz[b,e]azepin-5-yl)-carbonyl]-N-(2-methylphenyl)benzamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | O-Toluidine | HCID 7242 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 4-[(6,11-dihydro-5H-dibenz[b,e]azepin-5-yl)carbonyl]benzoyl chloride | HCID 53802244 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 4-[(6,11-Dihydro-5H-dibenz[b,e]azepin-5-yl)-carbonyl]-N-(2-methylphenyl)benzamide | HCID 15307991 | 5.8% |
Reaction Steps
To a mixture of 0.362 g of 4-[(6,11-dihydro-5H-dibenz[b,e]azepin-5-yl)carbonyl]benzoyl chloride and 0.101 g of triethylamine in 5 ml of dichloromethane is added a solution of 0.129 g of 2-methylaniline in 3 ml of dichloromethane. The mixture is stirred 1.5 hr at room temperature and then washed with H2O 1N HCl 1M NAHCO3, brine and dried (Na2SO4). The solvent is removed to give a solid. The solid is dissolved in dichloromethane and filtered through a thin pad of hydrous magnesium silicate with dichloromethane as eluent to give 0.025 g of crystals, m.p. 214°-216° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05834461 |
| Source dataset | uspto-grants-1998_11 |
| ORD ID | ord-1f5314339f0f463e98f4b3d4e5a0ed2b |
| Source note | uspto-grants-1998_11 |