Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Citric Acid | HCID 311 | — |
| Reactant | HCID 12434328 | HCID 12434328 | — |
| Reactant | Sodium Hypochlorite | HCID 23665760 | — |
| Reactant | Sodium Bisulfite | HCID 23665763 | — |
| Product | HCID 13670774 | HCID 13670774 | 49.7% |
Reaction Steps
2-Acetyl-4-(2-chlorophenyl)-9-methyl-6H-thieno[3,2-f] [1,2,4]triazolo[4,3-a] [1,4]diazepine (1.0 g) synthesized by the method described in Artneim.-Forsch./Drug Res. 28 (II), Heft 7, 1153-1158 (1978) was added to a 10% aqueous sodium hypochlorite solution (21 ml), and the mixture was stirred at 60° C. for 1.5 hours. Sodium hydrogensulfite (2.9 g) was added to the reaction mixture. Then, an aqueous citric acid solution was added to adjust the reaction mixture to pH 3. The obtained crystals were collected by filtration, and washed with water to give 0.5 g of (4-(2-chlorophenyl)-9-methyl-6H-thieno[3,2-f] [1,2,4]triazolo[4,3-a] [1,4]diazepin-2-yl)carboxylic acid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05760032 |
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| Source dataset | uspto-grants-1998_06 |
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| ORD ID | ord-9aa8df54cf804bc88edba53e3784374a |
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| Source note | uspto-grants-1998_06 |
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