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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1359582Generated: November 3, 2026

Sodium Chloride → 5-(4-chlorophenyl)-8-methyl-11H-1,3-dioxolo[4,5-h]imidazo[1,2-c][2,3]benzodiazepine

https://huagongshe.com/reaction/1359582

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium ChlorideHCID 5234—
ReactantSodium SulfiteHCID 24437—
Reactant5-(4-aminophenyl)-8-methyl-11H-1,3-dioxolo[4,5-h]imidazo[1,2-c][2,3]benzodiazepineHCID 18183170—
ReactantSodium NitriteHCID 23668193—
CatalystCopper sulfate pentahydrateHCID 24463—
SolventHydrochloric AcidHCID 313—
SolventWaterHCID 962—
Product5-(4-chlorophenyl)-8-methyl-11H-1,3-dioxolo[4,5-h]imidazo[1,2-c][2,3]benzodiazepineHCID 1818313451.4%

Reaction Steps

160 mg of 5-(4-aminophenyl)-8-methyl-11H-1,3-dioxolo[4,5-h]imidazo[1,2-c][2,3]benzodiazepine is dissolved in 2 ml of water and 2 ml of concentrated hydrochloric acid, and it is diazotized at 0° C. with a solution of 36 mg of sodium nitrite in 0.5 ml of water. Stirring is continued for 45 minutes at 0° C. To this solution at room temperature is added in drops a solution which is prepared as follows: 256 mg of copper sulfate pentahydrate is mixed in 1 ml of water with 87 mg of sodium chloride and mixed drop by drop with a solution of 68 mg of sodium sulfite in 0.6 ml of water. The white precipitate is separated from the supernatant by decanting, washed twice with water and dissolved in concentrated hydrochloric acid. After this solution is added, it is heated for 10 minutes in a steam bath and stirred for 1 more hour at room temperature. It is diluted with water, made alkaline with ammonia solution and extracted with ethyl acetate. The ethyl acetate phase is washed with saturated sodium chloride solution, dried, filtered and concentrated by evaporation. After chromatography on silica gel with methylene chloride:ethanol=10:1, 87 mg of 5-(4-chlorophenyl)-8-methyl-11H-1,3-dioxolo[4,5-h]imidazo[1,2-c][2,3]benzodiazepine is obtained.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06600036B2
Source datasetuspto-grants-2003_07
ORD IDord-a016a4c5a6e84fd185d5162d3760cf8a
Source noteuspto-grants-2003_07