HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1987582Generated: November 1, 2026
Pyridine → 4,4,4-Trifluoro-2-(4-fluoro-3-methyl-benzenesulfonylamino)-3-trifluoromethyl-butyric acid ethyl ester
https://huagongshe.com/reaction/1987582
Participants
| Role | Name | HCID | Charge |
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| Reactant | Pyridine | HCID 1049 | — |
| Reactant | 4-Fluoro-3-methylbenzene-1-sulfonyl chloride | HCID 2782758 | — |
| Reactant | 4,4,4,4',4',4'-Hexafluorovaline, ethyl ester | HCID 52991940 | — |
| Solvent | 1,1-Dichloroethane | HCID 6365 | — |
| Product | 4,4,4-Trifluoro-2-(4-fluoro-3-methyl-benzenesulfonylamino)-3-trifluoromethyl-butyric acid ethyl ester | HCID 86616007 | 64.7% |
Reaction Steps
To a vial containing a solution of 4-fluoro-3-methylbenzenesulfonyl chloride (50 mg, 0.24 mmol) and 2-amino-4,4,4-trifluoro-3-trifluoromethyl-butyric acid ethyl ester (61 mg, 0.24 mmol) in anhydrous dichloroethane (1 mL) was added pyridine (58 μL, 0.719 mmol). The vial was capped and shaken for 18 h. The solvent was removed in vacuo and the residue transferred to a separatory funnel with EtOAc (100 mL) and washed with distilled water (100 mL×2). The organic layer was removed and the combined aqueous washings were extracted with EtOAc (100 mL×2). The organic extracts were combined, washed with brine (100 mL), dried (MgSO4), filtered, and evaporated to give a white solid (66 mg). This material was purified by Gilson RP-HPLC (column YMC Combiprep 50×20 mm, gradient 10-100% CH3CN: H2O) to afford a white solid (29 mg, 28%). Mass Spectrum (−ESI): 424 [M−H]−.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07550629B2 |
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| Source dataset | uspto-grants-2009_06 |
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| ORD ID | ord-b5e6f40a4747459e82954a9e0640e8f9 |
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| Source note | uspto-grants-2009_06 |
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