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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1706615Generated: November 1, 2026

Water → 7-chloro-N-(2-chloroethyl)-5-(o-chlorophenyl)-2,3-dihydro-1H-1,4-benzodiazepine-1-carboxamide 4-oxide

https://huagongshe.com/reaction/1706615

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantHCID 20333751HCID 20333751—
SolventAcetic AcidHCID 176—
SolventPeracetic AcidHCID 6585—
Product7-chloro-N-(2-chloroethyl)-5-(o-chlorophenyl)-2,3-dihydro-1H-1,4-benzodiazepine-1-carboxamide 4-oxideHCID 20333771—

Reaction Steps

10 Parts of 7-chloro-N-(2-chloroethyl)-5-(o-chlorophenyl)-2,3-dihydro-1H-1,4-benzodiazepine-1-carboxamide is dissolved in 50 parts by volume of glacial acetic acid and to this solution 10 parts by volume of 40% peracetic acid is added all at once with stirring. The reaction mixture is stirred at ambient temperature for about 24 hours and then slowly poured into 1000 parts by volume of cold water. The precipitate which forms is extracted with methylene chloride, the extract dried over magnesium sulfate and the solvent removed. The residue crystallizes from ethanol to afford 7-chloro-N-(2-chloroethyl)-5-(o-chlorophenyl)-2,3-dihydro-1H-1,4-benzodiazepine-1-carboxamide 4-oxide. This compound is represented by the following formula ##STR37##

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04208327
Source datasetuspto-grants-1980_06
ORD IDord-d7ec9b7d409e4e5e9553896633efeee1
Source noteuspto-grants-1980_06