HuagongsheHuagongshe Chemistry Print Report · For research reference only
Benzaldehyde → HCID 53744844, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Benzaldehyde | HCID 240 | — |
| Reactant | HCID 21437113 | HCID 21437113 | — |
| Solvent | Benzene | HCID 241 | — |
| Product | HCID 53744844 | HCID 53744844 | 80.7% |
Reaction Steps
1 ml. (9.1 mmoles) of benzaldehyde is added to a solution of 2.0 g. (6.6 mmoles) of 1-methyl-4-amino-5-phenyl-7-chloro-1,3,4,5-tetrahydro-2H-1,4-benzodiazepine-2-one in 20 ml. of benzene, and the mixture is stirred at room temperature overnight. At the end of the reaction the mixture is evaporated to dryness under reduced pressure, the residue is triturated with 20 ml. of ether, and the solid substance is filtered off. 2.1 g. (80.7 %) of 1-methyl-4-benzalamino-5-phenyl-7-chloro-1,3,4,5-tetrahydro-2H-1,4-benzodiazepine-2-one are obtained. M.p.: 157°-158° C. (after recrystallization from ethanol). Rf(4) = 0.7.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04021421 |
| Source dataset | uspto-grants-1977_05 |
| ORD ID | ord-82f751149ca74ff28afe73c45d18614c |
| Source note | uspto-grants-1977_05 |