HuagongsheHuagongshe Chemistry Print Report · For research reference only
O-Toluidine → N-(2-Methylphenyl)-4-(5H-pyrrolo[2,1-c][1,4]-benzodiazepin-10(11H)-ylcarbonyl)benzamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | O-Toluidine | HCID 7242 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 4-(5H-pyrrolo[2,1-c]-[1,4]benzodiazepin-10(11H)-ylcarbonyl)benzoic acid | HCID 9905628 | — |
| Reactant | Diethylphosphorylcyanide | HCID 13586794 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | N-(2-Methylphenyl)-4-(5H-pyrrolo[2,1-c][1,4]-benzodiazepin-10(11H)-ylcarbonyl)benzamide | HCID 21836973 | 54.6% |
Reaction Steps
A mixture of 0.332 g of 4-(5H-pyrrolo[2,1-c][1,4]benzodiazepin-10(11H)-ylcarbonyl)benzoic acid, 0.111 g of triethylamine, 0.107 g of o-toluidine, and 0.15 ml of diethylphosphoryl cyanide in 20 ml of dichloromethane is heated on a steam bath overnight. The mixture is washed with water, 1 M NAHCO3, 1 N HCl, brine and dried (Na2SO4). The dichloromethane solution is filtered through a thin pad of hydrous magnesium silicate and the filtrate concentrated to dryness. The residue is crystallized from dichloromethane-hexane to give 0.23 g of white crystals, m.p. 228-231° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05968937 |
| Source dataset | uspto-grants-1999_10 |
| ORD ID | ord-abff1bc6881c478cb02deabe87225e99 |
| Source note | uspto-grants-1999_10 |