HuagongsheHuagongshe Chemistry Print Report · For research reference only
Acetic Acid → HCID 20329336, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Acetic Acid | HCID 176 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | HCID 20395211 | HCID 20395211 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 20329336 | HCID 20329336 | — |
Reaction Steps
3.5 g of 4-acetoxy-8-chloro-6-phenyl-4H-s-triazolo[4,3-a][1,5]benzodiazepin-5-one and 2.8 ml of 4N aqueous sodium hydroxide in 160 ml of ethanol are stirred overnight at 25°. The reaction is neutralized with 0.5 g of acetic acid and the solvent is evaporated. The residue is partitioned between chloroform and water, the organic phase is dried and the solvent evaporated to give the title compound.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04133809 |
| Source dataset | uspto-grants-1979_01 |
| ORD ID | ord-7a95e50296c649f39a741c80ff392246 |
| Source note | uspto-grants-1979_01 |