HuagongsheHuagongshe Chemistry Print Report · For research reference only
Sulfuric Acid → 6-phenyl-4H-s-triazolo[4,3-a][1,4-]benzodiazepine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Sulfuric Acid | HCID 1118 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | 2-hydrazino-5-phenyl-3H-1,4-benzodiazepine | HCID 12612389 | — |
| Reactant | Ethylorthoformate | HCID 53630039 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | 6-phenyl-4H-s-triazolo[4,3-a][1,4-]benzodiazepine | HCID 12562518 | — |
Reaction Steps
To a mixture of 1 part of 2-hydrazino-5-phenyl-3H-1,4-benzodiazepine, prepared in Example 3, 2 parts by volume of ethyl orthoformate and 20 parts by volume of ethanol, 0.44 part by volume of concentrated sulfuric acid is added dropwise with ice-cooling. The mixture is stirred at room temperature for 30 minutes and neutralized with saturated aqueous sodium bicarbonate. The resulting oily substance is extracted with methylene chloride. The methylene chloride layer is washed with water, dried over sodium sulfate and the solvent is evaporated, whereby 6-phenyl-4H-s-triazolo [4,3-a] [1,4] benzodiazepine is yielded as crystals. Recrystallization from a mixture of acetone and n-hexane yields colorless needles melting at 195° C to 196° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04116956 |
| Source dataset | uspto-grants-1978_09 |
| ORD ID | ord-d75dd46618774ce4b021bb57bed51574 |
| Source note | uspto-grants-1978_09 |