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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1820627Generated: November 2, 2026

1-Pentanesulfonyl chloride → HCID 11386162, compound

https://huagongshe.com/reaction/1820627

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-Pentanesulfonyl chlorideHCID 237555—
ReactantHCID 66905728HCID 66905728—
SolventPyridineHCID 1049—
SolventDichloromethaneHCID 6344—
ProductHCID 11386162HCID 113861624%

Reaction Conditions

Temperature25 °C

Reaction Steps

1-Pentanesulfonyl chloride (0.034 g, 0.30 mmol) was added slowly to a solution of [4-(5-aminopyridin-2-yl)piperazin-1-yl]-(2-trifluoromethylphenyl)methanone in pyridine (2 mL) at 0° C. The mixture was stirred at 25° C. for 16 hours and then diluted with dichloromethane. The organic phase was washed with water and saturated NaCl solution, dried over anhydrous MgSO4. After removal of dichloromethane, the product was purified by column chromatography to afford the title compound in 4% yield (2.7 mg). 1H NMR (300 MHz, CDCl3) δ 8.02, 7.87, 7.74, 7.61, 7.36, 6.94, 4.47, 4.11, 3.87, 3.68, 3.60, 3.42, 2.99, 1.77, 1.32, 0.88. MS (ES+) m/z 485.2 (M+1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07605161B2
Source datasetuspto-grants-2009_10
ORD IDord-997cbce137c94f1186545b9d8a68fa30
Source noteuspto-grants-2009_10