HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 965951Generated: October 27, 2026
Diethyl Ether → 5-[5-(4-bromophenyl)-4-chloro-3-(trifluoromethyl)-1H-pyrazol-1-yl]-2-pyridinesulfonamide
https://huagongshe.com/reaction/965951
Participants
| Role | Name | HCID | Charge |
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| Reactant | Diethyl Ether | HCID 3283 | — |
| Reactant | Sodium Thiosulfate | HCID 24477 | — |
| Reactant | Chlorosuccinimide | HCID 31398 | — |
| Reactant | 5-[5-(4-bromophenyl)-3-(trifluoromethyl)-1H-pyrazol-1-yl]-2-pyridinesulfonamide | HCID 12968617 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 5-[5-(4-bromophenyl)-4-chloro-3-(trifluoromethyl)-1H-pyrazol-1-yl]-2-pyridinesulfonamide | HCID 22313805 | 63% |
Reaction Steps
To a solution of 5-[5-(4-bromophenyl)-3-(trifluoromethyl)-1H-pyrazol-1-yl]-2-pyridinesulfonamide (350 mg, 0.783 mmol) in N,N-dimethylformamide (12 ml) was added N-chlorosuccinimide (1.05 g, 7.83 mmol) at room temperature. After the mixture was stirred for 18 hr, 1.05 g of N-chlorosuccinimide was added. The resulting mixture was stirred for further 36 hr. 20 nm of saturated aqueous sodium thiosulfate and 50 nm of diethyl ether were added and the two-phase-mixture was stirred for 0.5 hr. The separated organic layer was washed with water (20 ml×3) and dried over magnesium sulfate. Removal of solvent gave a pale yellow gum, which was chromatographed on a column of silica gel (50 g) eluting with ethyl acetate/hexane (1:3) to afford 236 mg (63%) of the title compound as a white solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06951876B2 |
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| Source dataset | uspto-grants-2005_10 |
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| ORD ID | ord-8880440d42fa484a92eacc4559145a44 |
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| Source note | uspto-grants-2005_10 |
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