HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1378093Generated: October 31, 2026
Chloroacetic anhydride → HCID 22914464, compound
https://huagongshe.com/reaction/1378093
Participants
| Role | Name | HCID | Charge |
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| Reactant | Chloroacetic anhydride | HCID 10946 | — |
| Reactant | HCID 67713563 | HCID 67713563 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 22914464 | HCID 22914464 | 61% |
Reaction Steps
9.4 g (34.7 mmol) of 5-methyl-6-oxo-5,6-dihydro-4H-imidazo[1,5-a][1,4]benzodiazepine-3-carboxylic acid hydrazide were stirred at room temperature for 3 hours in 75 ml of N,N-dimethyl- formamide with 27.1 g (41.5 mmol) of chloroacetic anhydride. After evaporating the solvent the residue was stirred at room temperature overnight with 75 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 6.9 g (61%) of 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. 221°-222°.
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-fa111943f86547f4904076e59292fd5d |
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| Source note | uspto-grants-1997_09 |
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