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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1049024Generated: October 31, 2026

Diisopropylethylamine → 4-{5-[(4-Fluoro-phenyl)-isobutyl-sulfamoyl]-pyridin-2-ylamino}-piperidine-1-carboxylic acid tert-butyl ester

https://huagongshe.com/reaction/1049024

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiisopropylethylamineHCID 81531—
ReactantSodium BicarbonateHCID 516892—
Reactant4-Amino-1-Boc-piperidineHCID 1268291—
Reactant6-Chloro-pyridine-3-sulfonic acid (4-fluoro-phenyl)-isobutyl-amideHCID 86721875—
SolventAcetonitrileHCID 6342—
SolventEthyl AcetateHCID 8857—
Product4-{5-[(4-Fluoro-phenyl)-isobutyl-sulfamoyl]-pyridin-2-ylamino}-piperidine-1-carboxylic acid tert-butyl esterHCID 8672187631%

Reaction Conditions

Temperature160 °C

Reaction Steps

To a solution of 6-chloro-pyridine-3-sulfonic acid (4-fluoro-phenyl)-isobutyl-amide (150 mg, 439 μmol) and 4-amino-1-boc piperidine (114 mg, 570 μmol) in acetonitrile (3 mL) was added DIPEA (115 μl, 658 μmol) and the reaction was heated at 160° C. in a microwave reactor for 2.5 hours. EtOAc and saturated aqueous NaHCO3 were added, extracted, washed with brine, dried with Na2SO4 then concentrated and purified by silica gel column chromatography (0-50% EtOAc in cyclohexane) to give 4-{5-[(4-fluoro-phenyl)-isobutyl-sulfamoyl]-pyridin-2-ylamino}-piperidine-1-carboxylic acid tert-butyl ester (69 mg, 31%). LCMS (m/z, Method A) ES− 506 [M−1]−.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09382222B2
Source datasetuspto-grants-2016_07
ORD IDord-9e998b1fde03419e8ab94903b300f7a4
Source noteuspto-grants-2016_07