HuagongsheHuagongshe Chemistry Print Report · For research reference only
Chlorophenyl isocyanate → 3-(2-Chlorophenylureido)-1,3-dihydro-5-(2,6-dimethoxy-4-methylphenyl)-1-methyl-1,4-benzodiazepin-2-one
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Chlorophenyl isocyanate | HCID 76833 | — |
| Reactant | 3-Amino-1,3-dihydro-5-(2,6-dimethoxy-4-methylphenyl)-1-methyl-1,4-benzodiazepin-2-one | HCID 15379622 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 3-(2-Chlorophenylureido)-1,3-dihydro-5-(2,6-dimethoxy-4-methylphenyl)-1-methyl-1,4-benzodiazepin-2-one | HCID 15388733 | 91% |
Reaction Steps
To 56 mg of 3-amino-1,3-dihydro-5-(2,6-dimethoxy-4-methylphenyl)-1-methyl-1,4-benzodiazepin-2-one in 10 ml of dichloromethane is added 0.022 ml of 2-chlorophenyl isocyanate and the reaction mixture is then stirred at room temperature overnight. It is concentrated under vacuum and the residue is crystallized from isopropyl ether to give 3-(2-chlorophenylureido)-1,3-dihydro-5-(2,6-dimethoxy-4-methylphenyl)-1-methyl-1,4-benzodiazepin-2-one; m.p.=260° C.; Yield=91%.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05719143 |
| Source dataset | uspto-grants-1998_02 |
| ORD ID | ord-5d16e6fd30564d4cae062e17e5739b3a |
| Source note | uspto-grants-1998_02 |