HuagongsheHuagongshe Chemistry Print Report · For research reference only
Acetic Acid → 8-chloro-4-(nitrosomethylamino)-1-phenyl-3H-1,5-benzodiazepin-2-one
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Acetic Acid | HCID 176 | — |
| Reactant | Sodium Nitrite | HCID 23668193 | — |
| Reactant | HCID 178482322 | HCID 178482322 | — |
| Solvent | Water | HCID 962 | — |
| Product | 8-chloro-4-(nitrosomethylamino)-1-phenyl-3H-1,5-benzodiazepin-2-one | HCID 178526374 | — |
Reaction Steps
A mixture of 6 g (0.02 mol) of 7-chloro-3,5-dihydro-2-methylamino-5-phenyl-4H-1,5-benzodiazepin-4-one, 25 ml of glacial acetic acid and 1.75 g (0.025 mol) of sodium nitrite was stirred stirred at 10°-20° for 1 hr. The reaction mixture was diluted with ice and water and stirred for another 15 min. The precipitated material was collected and dissolved in methylene chloride. The solution was washed with sodium bicarbonate solution, dried over sodium sulfate and evaporated. Crystallization from methylene chloride/hexane yielded the above-named product as yellow crystals, with mp 120°-125°. For analysis it was recrystallized like form methylene chloride/hexane, mp. 122°-125°.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04111934 |
| Source dataset | uspto-grants-1978_09 |
| ORD ID | ord-a590d9a4939d4f02855eb4a29ab472d7 |
| Source note | uspto-grants-1978_09 |