HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1897992Generated: October 29, 2026
4-Chloro-3-(trifluoromethyl)benzenesulfonyl Chloride → HCID 11583838, compound
https://huagongshe.com/reaction/1897992
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 4-Chloro-3-(trifluoromethyl)benzenesulfonyl Chloride | HCID 2780719 | — |
| Reactant | HCID 57942576 | HCID 57942576 | — |
| Solvent | Pyridine | HCID 1049 | — |
| Product | HCID 11583838 | HCID 11583838 | — |
Reaction Steps
To a solution of 5-chloro-2-(pyridin-4-ylsulfanyl)-pyridin-3-ylamine (100 mg, 0.42 mmol) in anhydrous pyridine (0.5 mL) was added drop wise a solution of 4-chloro-3-trifluoromethyl-benzenesulfonyl chloride (117 mg, 0.42 mmol) in pyridine (0.25 mL). The resulting mixture was stirred at room temperature for 2 days. The reaction mixture was concentrated under reduced pressure and diluted with EtOAc and brine. The aqueous portion was separated and extracted with EtOAc. The combined extracts were dried (Na2SO4) filtered and concentrated under reduced pressure. The residue was treated with 0.3 M aqueous NaOH and washed with CH2Cl2. The aqueous portion was acidified with conc HCl to pH 3 and extracted with EtOAc. The combined extracts were dried (Na2SO4) filtered and concentrated under reduced pressure. The residue was separated by preparative HPLC (20→80% gradient of ACN-water) and pure product fractions were lyophilized to provide pure product as a solid. Mass spectrum m/z: 480.0 (M+H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08519135B2 |
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| Source dataset | uspto-grants-2013_08 |
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| ORD ID | ord-a9fd058054f04301a1e0a1c261314fed |
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| Source note | uspto-grants-2013_08 |
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