HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1052927Generated: October 26, 2026
1-Hydroxybenzotriazole → 2-ethylsulfanyl-4-trifluoromethyl-N-(5-trifluoromethyl-pyri din-2-yl)-benzamide
https://huagongshe.com/reaction/1052927
Participants
| Role | Name | HCID | Charge |
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| Reactant | 1-Hydroxybenzotriazole | HCID 75771 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | 2-Amino-5-(trifluoromethyl)pyridine | HCID 735862 | — |
| Reactant | 1,3-Propanediamine, N'-(ethylcarbonimidoyl)-N,N-dimethyl-, monohydrochloride | HCID 2723939 | — |
| Reactant | 2-(Ethylthio)-4-(trifluoromethyl)benzoic acid | HCID 91876372 | — |
| Solvent | Pyridine | HCID 1049 | — |
| Product | 2-ethylsulfanyl-4-trifluoromethyl-N-(5-trifluoromethyl-pyri din-2-yl)-benzamide | HCID 118035097 | 65% |
Reaction Steps
A mixture of 1.62 g of 2-amino-5-trifluoromethylpyridine, 2.5 g of 2-ethylsulfanyl-4-trifluoromethylbenzoic acid, 2.3 g of EDCI hydrochloride, 0.13 g of HOBt and 5 mL of pyridine was stirred at room temperature for 2 hours and at 60° C. for 1 hour. A saturated aqueous sodium bicarbonate solution was added to the cooled reaction mixture, and the mixture was extracted with ethyl acetate. The organic layer was dried over anhydrous sodium sulfate and then concentrated under reduced pressure, and the resulting residue was applied to a silica gel column chromatography to obtain 2.56 g of 2-ethylsulfanyl-4-trifluoromethyl-N-(5-trifluoromethyl-pyridin-2-yl)-benzamide.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09392791B2 |
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| Source dataset | uspto-grants-2016_07 |
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| ORD ID | ord-2cb9444d3b4547088d144d19f3398ee6 |
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| Source note | uspto-grants-2016_07 |
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