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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 963053Generated: October 26, 2026

Sulfuric Acid → N-(3-bromo-4-(3-(2-chlorobenzoyl)-5-ethylthiophen-2-yl) [1,2,4]triazol-5-ylmethyl)-3,4-dichlorobenzamide

https://huagongshe.com/reaction/963053

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSulfuric AcidHCID 1118—
ReactantBenzoyl chloride, 3,4-dichloro-HCID 76403—
ReactantSodium BicarbonateHCID 516892—
Reactant9-Bromo-4-(2-chlorophenyl)-2-ethyl-6H-thieno[3,2-f] [1,2,4]triazolo[4,3-a] [1,4]diazepineHCID 67727685—
SolventChloroformHCID 6212—
ProductN-(3-bromo-4-(3-(2-chlorobenzoyl)-5-ethylthiophen-2-yl) [1,2,4]triazol-5-ylmethyl)-3,4-dichlorobenzamideHCID 67728033—

Reaction Conditions

Temperature80 °C

Reaction Steps

9-Bromo-4-(2-chlorophenyl)-2-ethyl-6H-thieno[3,2-f] [1,2,4]triazolo[4,3-a] [1,4]diazepine is added to 2M sulfuric acid, and the mixture is stirred at 80° C. overnight. Sodium hydrogencarbonate is added to the reaction mixture to make the mixture alkaline. Chloroform and 3,4-dichlorobenzoyl chloride are added, and the mixture is stirred at room temperature for 2 hours to give N-(3-bromo-4-(3-(2-chlorobenzoyl)-5-ethylthiophen-2-yl) [1,2,4]triazol-5-ylmethyl)-3,4-dichlorobenzamide.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05760032
Source datasetuspto-grants-1998_06
ORD IDord-206e6a62da7f43c9be0a11c43a705388
Source noteuspto-grants-1998_06