HuagongsheHuagongshe Chemistry Print Report · For research reference only
Chlorosuccinimide → HCID 23317233, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Chlorosuccinimide | HCID 31398 | — |
| Reactant | HCID 12923439 | HCID 12923439 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 23317233 | HCID 23317233 | 117.2% |
Reaction Steps
4.1 g of 1-methyl-2-chloromethyl-5-phenyl-2,3-dihydro-1H-1,4-benzodiazepine and 1.94 g of N-chlorosuccinimide were heated under reflux in 50 ml methylenechloride for 24 hours. The solvent was then distilled off in a vacuum, the crude product was taken up in ether and reacted with an isopropanol solution of hydrogen chloride. There were obtained 3 g of 7-chloro-1-methyl-2-chloromethyl-5-phenyl-2,3-dihydro-1H-1,4-benzodiazepine hydrochloride. The product was identical with that of Example 4.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04096141 |
| Source dataset | uspto-grants-1978_06 |
| ORD ID | ord-c0176924b43d40549e5370d77853bce5 |
| Source note | uspto-grants-1978_06 |