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
Participants
| Role | Name | HCID | Charge |
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| Reactant | Sulfuric Acid | HCID 1118 | — |
| Reactant | Benzoyl chloride, 3,4-dichloro- | HCID 76403 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | 9-Bromo-4-(2-chlorophenyl)-2-ethyl-6H-thieno[3,2-f] [1,2,4]triazolo[4,3-a] [1,4]diazepine | HCID 67727685 | — |
| Solvent | Chloroform | HCID 6212 | — |
| Product | N-(3-bromo-4-(3-(2-chlorobenzoyl)-5-ethylthiophen-2-yl) [1,2,4]triazol-5-ylmethyl)-3,4-dichlorobenzamide | HCID 67728033 | — |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05760032 |
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| Source dataset | uspto-grants-1998_06 |
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| ORD ID | ord-206e6a62da7f43c9be0a11c43a705388 |
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| Source note | uspto-grants-1998_06 |
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