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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1049047Generated: October 31, 2026

Diisopropylethylamine → 1-Methanesulfonyl-piperidine-4-carboxylic acid {4-[isobutyl-(2-trifluoromethyl-phenyl)-sulfamoyl]-phenyl}-amide

https://huagongshe.com/reaction/1049047

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiisopropylethylamineHCID 81531—
Reactant1-Methanesulfonylpiperidine-4-carbonyl chlorideHCID 12115993—
Reactant4-amino-N-isobutyl-N-(2-trifluoromethyl-phenyl)-benzenesulfonamideHCID 86721891—
SolventDichloromethaneHCID 6344—
Product1-Methanesulfonyl-piperidine-4-carboxylic acid {4-[isobutyl-(2-trifluoromethyl-phenyl)-sulfamoyl]-phenyl}-amideHCID 8672189265.1%

Reaction Steps

A solution of 4-amino-N-isobutyl-N-(2-trifluoromethyl-phenyl)-benzenesulfonamide (100 mg, 0.268 mmol), 1-(methylsulfonyl)-4-piperidinecarbonyl chloride (108 mg, 0.48 mmol) and DIPEA (138 μL, 0.804 mmol) in DCM (8 mL) was stirred at room temperature for 3 hours. The mixture was diluted with DCM, washed with 1 N aqueous HCl, saturated aqueous NaHCO3, water and brine, dried over Na2SO4 and concentrated under vacuum. Purification by silica gel column chromatography (0-100% EtOAc in cyclohexane) and triturating with Et2O/pentane gave the title compound (98 mg, 65%). 1H NMR (400 MHz, DMSO δ 10.42 (s, 1H), 7.85 (d, J=8.8 Hz, 2H), 7.82 (dd, J=7.7, 1.9 Hz, 1H), 7.62-7.63 (m, 1H), 7.58 (d, J=8.8 Hz, 2H), 6.99 (d, J=7.8 Hz, 1H), 3.63 (d, J=11.8 Hz, 2H), 3.38-3.39 (m, 1H), 3.11 (dd, J=13.4, 4.7 Hz, 1H), 2.90 (s, 3H), 2.76-2.78 (m, 2H), 1.95 (d, J=13.5 Hz, 2H), 1.63-1.68 (m, 2H), 1.44-1.48 (m, 1H), 1.09 (t, J=7.0 Hz, 1H), 0.88 (d, J=6.5 Hz, 3H), 0.71 (d, J=6.7 Hz, 3H). LCMS (m/z, Method B) ES+ 562.0 [M+1]+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09382222B2
Source datasetuspto-grants-2016_07
ORD IDord-ede15370735e40ebb67e5976d86d4d88
Source noteuspto-grants-2016_07