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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 963039Generated: October 29, 2026

Hydrochloric Acid → HCID 19085375, compound

https://huagongshe.com/reaction/963039

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantBenzoyl chloride, 3,4-dichloro-HCID 76403—
ReactantSodium BicarbonateHCID 516892—
ReactantHCID 67727704HCID 67727704—
SolventChloroformHCID 6212—
ProductHCID 19085375HCID 19085375—

Reaction Conditions

Temperature70 °C

Reaction Steps

4-(2-Chlorophenyl)-2-ethyl-9-trifluoromethyl-6H-thieno[3,2-f] [1,2,4]triazolo[4,3-a] [1,4]diazepine (1.0 g) was added to 10% hydrochloric acid (20 ml), and the mixture was stirred at 70° C. overnight. Then, sodium hydrogencarbonate was added to the reaction mixture to make the mixture alkaline. Chloroform (20 ml) and 3,4-dichlorobenzoyl chloride (0.58 g) were added, and the mixture was stirred under ice-cooling for 1 hour. Then, the organic layer was washed with an aqueous citric acid solution, a saturated aqueous sodium hydrogencarbonate solution and saturated brine, and dried over magnesium sulfate. The solvent was evaporated, and the residue was recrystallized from ethyl acetate-hexane to give 0.60 g of N-(4-(3-(2-chlorobenzoyl)-5-ethylthiophen-2-yl)-5-trifluoromethyl[1,2,4]triazol-3-ylmethyl)-3,4-dichlorobenzamide.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05760032
Source datasetuspto-grants-1998_06
ORD IDord-0653b4ec993b4abb98963960eefc6550
Source noteuspto-grants-1998_06