HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 963054Generated: October 25, 2026
Sulfuric Acid → N-(3-bromo-4-(3-(2-chlorobenzoyl)-5-ethylthiophen-2-yl) [1,2,4]triazol-5-ylmethyl)indole-2-carboxamide
https://huagongshe.com/reaction/963054
Participants
| Role | Name | HCID | Charge |
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| Reactant | Sulfuric Acid | HCID 1118 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | 1H-indole-2-carbonyl Chloride | HCID 11816208 | — |
| 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)indole-2-carboxamide | HCID 67727841 | — |
Reaction Steps
9-Bromo-4-(2-chlorophenyl)-2-ethyl-6H-thieno[3,2-f] [1,2,4]triazolo[4,3-a] [1,4]diazepine (1.0 g) was added to 2M sulfuric acid (26.5 ml), and the mixture was stirred at 80° C. overnight. Sodium hydrogencarbonate was added to the reaction mixture to make the mixture alkaline. Chloroform and indole-2-carbonyl chloride were added, and the mixture was stirred at room temperature for 1.5 hours. The obtained crystals were filtered and washed with ethyl acetate to give 0.196 g of N-(3-bromo-4-(3-(2-chlorobenzoyl)-5-ethylthiophen-2-yl) [1,2,4]triazol-5-ylmethyl)indole-2-carboxamide.
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-7f8e78b59ae244438656eda8002df5eb |
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| Source note | uspto-grants-1998_06 |
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