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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1639599Generated: November 2, 2026

Sodium Thiosulfate → N-[2-fluoro-3-(5H-pyrrolo[2,3-b]pyrazine-7-carbonyl)-phenyl]-4-trifluoromethyl-benzenesulfonamide

https://huagongshe.com/reaction/1639599

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium ThiosulfateHCID 24477—
ReactantTriacetoxyperiodinaneHCID 159087—
ReactantSodium BicarbonateHCID 516892—
ReactantN-{2-fluoro-3-[hydroxy-(5H-pyrrolo[2,3-b]pyrazin-7-yl)-methyl]-phenyl}-4-trifluoromethyl-benzenesulfonamideHCID 58001697—
SolventTetrahydrofuranHCID 8028—
ProductN-[2-fluoro-3-(5H-pyrrolo[2,3-b]pyrazine-7-carbonyl)-phenyl]-4-trifluoromethyl-benzenesulfonamideHCID 4453888075.4%

Reaction Steps

To N-{2-fluoro-3-[hydroxy-(5H-pyrrolo[2,3-b]pyrazin-7-yl)-methyl]-phenyl}-4-trifluoromethyl-benzenesulfonamide (27, 141 mg, 0.30 mmol) in 2 mL of tetrahydrofuran, Dess-Martin periodane (141 mg, 0.33 mmol) and sodium bicarbonate (200 mg) were added. The reaction was stirred at room temperature for one hour, then poured into saturated aqueous sodium thiosulfate solution and extracted with ethyl acetate. The organic layer was washed with brine, dried over anhydrous sodium sulfate, filtered and the filtrate concentrated under vacuum. The resulting material was purified by silica gel column chromatography eluting with 50%) ethyl acetate in hexane. Appropriate fractions were combined and concentrated under vacuum to provide the desired compound (P-0009, 105 mg, 75%). MS (ESI) [M−H+]−=463.4.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08110576B2
Source datasetuspto-grants-2012_02
ORD IDord-eea471f5b49c434f8ba7df9d2c062e46
Source noteuspto-grants-2012_02