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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2167984Generated: October 26, 2026

Diisopropylamine → 4-(1-(2,2-Difluoroethyl)piperidin-4-ylamino)-3-nitrobenzenesulfonamide

https://huagongshe.com/reaction/2167984

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiisopropylamineHCID 7912—
Reactant1,1-Difluoro-2-iodoethaneHCID 3833565—
ReactantHCID 67170227HCID 67170227—
SolventDimethylformamideHCID 6228—
SolventDichloromethaneHCID 6344—
Product4-(1-(2,2-Difluoroethyl)piperidin-4-ylamino)-3-nitrobenzenesulfonamideHCID 48934007—

Reaction Conditions

Temperature85 °C

Reaction Steps

3-nitro-4-(piperidin-4-ylamino)benzenesulfonamide hydrochloride (0.100 g), 1,1-difluoro-2-iodoethane (0.063 mL) and diisopropylamine (0.156 mL) were stirred together in N,N-dimethylformamide (3 ml) and heated to 85° C. The reaction was diluted with dichloromethane (50 mL) and washed with water (50 mL), brine (50 mL), dried over magnesium sulfate, filtered, and concentrated. The residue was loaded onto silica gel (GraceResolve 12 g) and eluted using a gradient of 0.5% methanol/dichloromethane to 3% methanol/dichloromethane over 30 minutes to give the title compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09045475B2
Source datasetuspto-grants-2015_06
ORD IDord-0c9557057d7a4e4f88c82d65a3d50788
Source noteuspto-grants-2015_06