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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 963035Generated: October 30, 2026

Hydrochloric Acid → HCID 19085362, compound

https://huagongshe.com/reaction/963035

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantBenzoyl chloride, 3,4-dichloro-HCID 76403—
ReactantSodium BicarbonateHCID 516892—
ReactantHCID 12434326HCID 12434326—
SolventChloroformHCID 6212—
ProductHCID 19085362HCID 19085362—

Reaction Conditions

Temperature60 °C

Reaction Steps

4-(2-Chlorophenyl)-2,9-diethyl-6H-thieno[3,2-f] [1,2,4]triazolo[4,3-a] [1,4]diazepine (1.8 g) was added to 2.5% hydrochloric acid (35 ml), and the mixture was stirred at 60° C. overnight. Then, sodium hydrogencarbonate was added to the reaction mixture to make the mixture alkaline. Chloroform (40 ml) and 3,4-dichlorobenzoyl chloride (1.15 g) were added, and the mixture was stirred at room temperature for 2 hours. Then, the organic layer was washed with an aqueous citric acid solution and saturated brine, and dried over magnesium sulfate. After the solvent was evaporated, the residue was purified by silica gel column chromatography (developing solvent:ethyl acetate) and recrystallized from ethyl acetate to give 0.73 g of N-(4-(3-(2-chlorobenzoyl)-5-ethylthiophen-2-yl)-5-ethyl[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-8dbd5e0ee84240d786012d441cf3fa36
Source noteuspto-grants-1998_06