HuagongsheHuagongshe Chemistry Print Report · For research reference only
Water → HCID 12434308, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Acetohydrazide | HCID 14039 | — |
| Reactant | HCID 135848425 | HCID 135848425 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 12434308 | HCID 12434308 | — |
Reaction Steps
1.5 g (0.00582 mol) of 1,3-dihydro-5-phenyl-2H-thieno[2,3-e]-1,4-diazepine-2-thione are heated to reflux for 4 hours under a nitrogen atmosphere with 1.3 g (0.0175 mol) of acetyl hydrazine in 120 ml of absolute ethanol. The solvent is evaporated and the crystals obtained are shaken with water in a separating funnel. After filtration under a vacuum, the product is recrystallized from ethyl acetate containing active carbon to give colorless crystals of 2-(2-acetylhydrazino)-5-phenyl-3H-thieno[2,3-e]-1,4-diazepine, melting point 194°-196° C. (transition).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04155913 |
| Source dataset | uspto-grants-1979_05 |
| ORD ID | ord-bc8f5b758ef74f78b82c2e411193a74f |
| Source note | uspto-grants-1979_05 |