HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1378096Generated: October 31, 2026
Chloroacetic anhydride → HCID 22914481, compound
https://huagongshe.com/reaction/1378096
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Chloroacetic anhydride | HCID 10946 | — |
| Reactant | 7-chloro-5-methyl-6-oxo-5,6-dihydro-4H-imidazo[1,5-a][1,4]benzodiazepin-3-carboxylic acid hydrazide | HCID 54382386 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 22914481 | HCID 22914481 | 53.3% |
Reaction Steps
15.3 g (50 mmol) of 7-chloro-5-methyl-6-oxo-5,6-dihydro-4H-imidazo[1,5-a][1,4]benzodiazepin-3-carboxylic acid hydrazide were stirred at room temperature overnight in 160 ml of N,N-dimethylformamide with 9.41 g (55 mmol) of chloroacetic anhydride. After evaporating the solvent the residue was stirred at room temperature over the weekend with 100 ml of a 10% solution of phosphorus pentoxide in methanesulphonic acid. The reaction mixture was treated with ice, made alkaline with conc. sodium hydroxide solution and extracted four times with methylene chloride. By drying the organic phase over magnesium sulfate, evaporation of the solvent and chromatography of the residue on silica gel while eluting with ethyl acetate there were obtained 9.7 g (53%) of 7-chloro-3-(5-chloromethyl-1,3,4-oxadiazol-2-yl)-5-methyl-5,6-dihydro-4H-imidazo[1,5-a][1,4]benzodiazepin-6-one of m.p. 201°-203°.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05665718 |
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| Source dataset | uspto-grants-1997_09 |
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| ORD ID | ord-f41fdb2ffbaf4857aa3dd9e5c86d577f |
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| Source note | uspto-grants-1997_09 |
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