HuagongsheHuagongshe Chemistry Print Report · For research reference only
7-chloro 5-(2-chlorophenyl)-1,3-dihydro-2H-(1,4)-benzodiazepine-2-thione → HCID 178521284, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 7-chloro 5-(2-chlorophenyl)-1,3-dihydro-2H-(1,4)-benzodiazepine-2-thione | HCID 826703 | — |
| Reactant | HCID 21497500 | HCID 21497500 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 178521284 | HCID 178521284 | 84% |
Reaction Steps
A suspension of 7-chloro-1,3-dihydro-5-(o-chlorophenyl)-2H-1,4-benzodiazepine-2-thione (18g, 56 mmole) and (3-phthalimidoacetonyl)amine, ethylene ketal (28.88 g, 112mmole) in 800 ml. of absolute ethanol is heated on a steambath, under nitrogen for 24 hours. The above mixture is then evaporated to dryness in vacuo to give 27 g (84%) of 7-chloro-5-(o-chlorophenyl)-2-[(3-phthalimidoacetonyl)amino]-3H-1,4-benzodiazepine, ethylene ketal as a buff-colored compound of melting point 180°-190° C. An analytical sample recrystallized from methanol ethyl acetate has a melting point of 200°-202° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US03992408 |
| Source dataset | uspto-grants-1976_11 |
| ORD ID | ord-5ba2d09b36744680bc6012777b4e4492 |
| Source note | uspto-grants-1976_11 |