HuagongsheHuagongshe Chemistry Print Report · For research reference only
Bromazepam → HCID 178482308, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Bromazepam | HCID 2441 | — |
| Reactant | Methylamine | HCID 6329 | — |
| Reactant | Tetrahydrofuran | HCID 8028 | — |
| Catalyst | Titanium Tetrachloride | HCID 24193 | — |
| Solvent | Benzene | HCID 241 | — |
| Product | HCID 178482308 | HCID 178482308 | — |
Reaction Steps
A solution of 63.2 g. (0.2 mol) of 7-bromo-1,3-dihydro-5-(2-pyridyl)-2H-1,4-benzodiazepin-2-one in 1.7 l. of tetrahydrofuran and 400 ml. of benzene was saturated with methylamine. A solution of 45.5 g. of titanium tetrachloride in 400 ml. of benzene was added slowly with ice cooling. After addition was complete, the reaction mixture was stirred and refluxed for 2 hours. It was then partitioned between water and methylene chloride. The organic layer was dried over sodium sulfate and evaporated. Crystallization from methylene chloride/hexane yielded 7-bromo-2-methylamino-5-(2-pyridyl)-3H-1,4-benzodiazepine, having a melting point of 208°-214°.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04044016 |
| Source dataset | uspto-grants-1977_08 |
| ORD ID | ord-2063d476d8b24d908c9292f350843698 |
| Source note | uspto-grants-1977_08 |