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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1689845Generated: November 1, 2026

1-Pentanesulfonyl chloride → HCID 11386162, compound

https://huagongshe.com/reaction/1689845

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 numberUS08153636B2
Source datasetuspto-grants-2012_04
ORD IDord-ef664399341d44b5a0c1e74083654245
Source noteuspto-grants-2012_04