HuagongsheHuagongshe Chemistry Print Report · For research reference only
2-Hydroxypropanehydrazide → 2-chloro-4-(o-chlorophenyl)-9-(alpha-hydroxyethyl)-6H-thieno[3,2-f]-s-triazolo[4,3-a][1,4]diazepine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 2-Hydroxypropanehydrazide | HCID 312043 | — |
| Reactant | 7-Chloro-5-(2-chlorophenyl)-1,3-dihydro-2H-thieno-(2,3-e)-(1,4)-diazepine-2-thione | HCID 135783078 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | 2-chloro-4-(o-chlorophenyl)-9-(alpha-hydroxyethyl)-6H-thieno[3,2-f]-s-triazolo[4,3-a][1,4]diazepine | HCID 21317675 | — |
Reaction Steps
1 g of 7-chloro-5-(o-chlorophenyl)-1,3-dihydro-2H-thieno[2,3-e]-1,4-diazepine-2-thione is refluxed for 1.5 hours in 50 ml of absolute methanol with 2 g of lactic acid hydrazide. The precipitated 7-chloro-5-(o-chlorophenyl)-2-(2-lactoylhydrazino)-3H-thieno[2,3-e]-1,4-diazepine is dried and refluxed for 4 hours in 120 ml of absolute xylene. The solution is evaporated and the product recrystallized from ethyl acetate containing active carbon to yield 2-chloro-4-(o-chlorophenyl)-9-(α-hydroxyethyl)-6H-thieno[3,2-f]-s- triazolo[4,3-a][1,4]diazepine of melting point 118°-120° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04155913 |
| Source dataset | uspto-grants-1979_05 |
| ORD ID | ord-406a2536ca584892889ddd9beae8b76c |
| Source note | uspto-grants-1979_05 |