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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1487049Generated: October 29, 2026

Sodium hydride → HCID 72189588, compound

https://huagongshe.com/reaction/1487049

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium hydrideHCID 24758—
Reactant[1-(2,2,2-Trifluoroethyl)piperidin-4-yl]methanolHCID 52274441—
ReactantHCID 89479332HCID 89479332—
SolventDimethyl SulfoxideHCID 679—
ProductHCID 72189588HCID 72189588—

Reaction Conditions

Temperature20 °C

Reaction Steps

To a solution of N-(2,4-dimethylphenyl)-4-fluoro-N-isobutylbenzenesulfonamide (25 mg, 0.075 mmol) and (1-(2,2,2-trifluoroethyl)piperidin-4-yl)methanol (14.70 mg, 0.075 mmol) in dimethyl sulfoxide (DMSO) (0.5 mL) stirred in air at 20° C., was added sodium hydride (approximately 2.98 mg, 0.075 mmol, 60% dispersed in oil) in one charge. The reaction mixture was stirred at 20° C. for 16 hours. The reaction was carefully quenched with methanol (0.5 mL) and water (0.5 mL). The solvent was concentrated in vacuo (Biotage V10) to give the crude product in DMSO (0.5 mL). The residue was taken up in additional DMSO (0.5 mL) and methanol (1 mL) then purified by mass directed autoprep (formic acid modifier). The appropriate fractions were evaporated under a stream of nitrogen to give the required product, 11.5 mg. LCMS [LCMS1] Rt 1.51 min, m/z (ES+) 513 (M+H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09428452B2
Source datasetuspto-grants-2016_08
ORD IDord-55d549140d3140a2980348d56ed3bfe7
Source noteuspto-grants-2016_08