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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1438647Generated: November 2, 2026

Water → HCID 57942414, compound

https://huagongshe.com/reaction/1438647

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantSodium borohydrideHCID 4311764—
ReactantHCID 57942176HCID 57942176—
SolventMethanolHCID 887—
ProductHCID 57942414HCID 57942414—

Reaction Steps

A mixture of 4-chloro-N-[5-chloro-2-(4-oxo-piperidine-1-carbonyl)-pyridin-3-yl]-3-trifluoromethyl-benzenesulfonamide (20 mg), sodium borohydride (10 mg) in 1 mL of methanol was stirred at room temperature overnight. To the mixture was added water and the resulting mixture was extracted with ethyl acetate three times. The organic layer was washed with brine and dried. After the removal of solvents the residue was further purified by flash column (50% ethyl acetate in hexane) to afford the title compound as a white solid: 1H NMR: (CDCl3, ppm) δ 8.12 (d, 1 H), 8.09 (d, 1 H), 7.95 (dd, 1 H), 7.80 (d, 1 H), 7.62 (d, 1 H), 4.05 (m, 1 H), 3.88 (m, 1 H), 3.47 (m, 1 H), 3.36 (m, 1 H), 3.02 (m, 1 H), 1.94 (m, 1 H), 1.73 (m, 1 H), 1.58(m, 1 H), 1.48 (m, 2H); MS: (M+H)/z=498.0.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07622583B2
Source datasetuspto-grants-2009_11
ORD IDord-130be504a8ca4009ba6a4b0c3b0626f0
Source noteuspto-grants-2009_11