HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 963044Generated: October 30, 2026
2-Naphthalenesulfonyl chloride → HCID 67727807, compound
https://huagongshe.com/reaction/963044
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 2-Naphthalenesulfonyl chloride | HCID 7125 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | HCID 22439190 | HCID 22439190 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 67727807 | HCID 67727807 | 70.3% |
Reaction Steps
3-Aminomethyl-4-(3-(2-chlorobenzoyl)-5-ethylthiophen-2-yl) [1,2,4]triazole di-p-toluenesulfonate (5.0 g) was dissolved in dimethylformamide (20 ml). 2-Naphthalenesulfonyl chloride (1.8 g) and triethylamine (5.0 ml) were added under ice-cooling, and the mixture was stirred at room temperature for 5 hours. A saturated aqueous sodium hydrogencarbonate solution was added to the reaction mixture, and the mixture was extracted with ethyl acetate. The organic layer was washed with an aqueous citric acid solution and then saturated brine, and dried over magnesium sulfate. The solvent was evaporated, and the residue was recrystallized from ethyl acetate to give 2.73 g of N-(4-(3-(2-chlorobenzoyl)-5-ethylthiophen-2-yl) [1,2,4]triazol-3-ylmethyl)naphthalene-2-sulfonamide.
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-058d8d7f6ea944788697a67dd2f74ca6 |
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| Source note | uspto-grants-1998_06 |
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