HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1594323Generated: October 27, 2026
Pyridine → 4,5-dichloro-N-[3,3,3-trifluoro-1-(hydroxymethyl)-2-(trifluoromethyl)propyl]thiophene-2-sulfonamide
https://huagongshe.com/reaction/1594323
Participants
| Role | Name | HCID | Charge |
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| Reactant | Pyridine | HCID 1049 | — |
| Reactant | 4,5-Dichlorothiophene-2-sulfonyl chloride | HCID 518622 | — |
| Reactant | 3,3,3-Trifluoro-2-(trifluoromethyl)-1-(hydroxymethyl)propylamine | HCID 45107971 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 4,5-dichloro-N-[3,3,3-trifluoro-1-(hydroxymethyl)-2-(trifluoromethyl)propyl]thiophene-2-sulfonamide | HCID 11189493 | 9% |
Reaction Steps
A solution of 3,3,3-trifluoro-2-(trifluoromethyl)-1-(hydroxymethyl)propylamine (0.192 g, 0.9 mmol) in THF (1 mL) was stirred under nitrogen at 25° C. Pyridine (0.147 mL, 1.82 mmol) was added followed by 4,5-dichlorothiophene-2-sulfonyl chloride (0.226 g, 0.391 mmol) in THF (1 mL), and the resulting solution stirred for 18 h at 25° C. After concentration, the residue was taken up in EtOAc (15 mL) and washed with 1 N aq. HCl (10 mL), brine (10 mL), and then dried (Na2SO4). After concentration, the crude product was purified by preparatory TLC, eluent: 30:70 EtOAc:hexanes, to provide 4,5-dichloro-N-[3,3,3-trifluoro-1-(hydroxymethyl)-2-(trifluoromethyl)propyl]thiophene-2-sulfonamide as a white solid (0.037 g, 9% yield, racemic mixture). Mass Spectrum (−ESI): 423.9 (M−H)−.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07300951B2 |
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| Source dataset | uspto-grants-2007_11 |
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| ORD ID | ord-31b68b7a72cf4ea6a5afd48f73587c83 |
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| Source note | uspto-grants-2007_11 |
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