HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 48347Generated: October 28, 2026
Acetic Anhydride → HCID 69892358, compound
https://huagongshe.com/reaction/48347
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Acetic Anhydride | HCID 7918 | — |
| Reactant | HCID 69892837 | HCID 69892837 | — |
| Solvent | Pyridine | HCID 1049 | — |
| Product | HCID 69892358 | HCID 69892358 | — |
Reaction Steps
50 mg (0.158 mmol) of (E)-5-(3,4-dichlorostyryl)-2,3-dihydro-1H-benzo-1,4-diazepine were dissolved in a mixture of 0.1 ml of acetic anhydride and 1 ml of pyridine by heating to 80° C. The mixture was left to cool for 30 minutes then evaporated to dryness and the residue dissolved in water and ethyl acetate. The organic phase was dried over magnesium sulphate, filtered, evaporated to dryness and the residue chromatographed on silica gel using ethyl acetate for the elution. The product was dissolved in a solution of hydrogen chloride in ethyl acetate, evaporated to dryness and the residue dissolved in a small volume of acetone and left to crystallize. There was obtained 12 mg of (E)-1-acetyl-5-(3,4-dichlorostyryl)-2,3-dihydro-1H-1,4-benzodiazepine hydrochloride as an off-white solid. MS: m/e 358.9 [M+H]+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06703387B2 |
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| Source dataset | uspto-grants-2004_03 |
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| ORD ID | ord-3a1809874ceb4c3391ab71e1fb01ff82 |
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| Source note | uspto-grants-2004_03 |
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