HuagongsheHuagongshe Chemistry Print Report · For research reference only
Acetic Acid → HCID 21564649, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Acetic Acid | HCID 176 | — |
| Reactant | 2-Mercaptoethanol | HCID 1567 | — |
| Reactant | Desmethylmedazepam | HCID 15539 | — |
| Reactant | 3H-1,4-Benzodiazepine, 7-chloro-5-phenyl- | HCID 27855 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 21564649 | HCID 21564649 | — |
Reaction Steps
7-chloro-2,3-dihydro-5-phenyl-1H-1,4-benzodiazepine (10 g) was oxidized to 7-chloro-5-phenyl-3H-1,4-benzodiazepine as described in Example 1 with the addition of 0.1 ml of acetic acid. The crude oxidation product was taken up in THF (60 ml), treated with 2-mercaptoethanol (10 ml ) and heated under reflux overnight. The resulting solution was concentrated under reduced pressure until the product began to crystallize and then diluted with 100 ml of ether. The product was collected and washed with ether to give the above-named product as colorless crystals, mp 135°-140° (dec).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US03932399 |
| Source dataset | uspto-grants-1976_01 |
| ORD ID | ord-f1aaf2d876ba49a9ad4bd27d8f2fb52e |
| Source note | uspto-grants-1976_01 |