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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1043072Generated: October 27, 2026

4-Chloro-3-nitrobenzenesulfonamide → 4-(1-Isopropylpiperidin-4-ylamino)-3-nitrobenzenesulfonamide

https://huagongshe.com/reaction/1043072

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-Chloro-3-nitrobenzenesulfonamideHCID 7324—
Reactant1-(Propan-2-yl)piperidin-4-amineHCID 3163333—
Solvent1,4-DioxaneHCID 31275—
Product4-(1-Isopropylpiperidin-4-ylamino)-3-nitrobenzenesulfonamideHCID 67422519—

Reaction Conditions

Temperature90 °C

Reaction Steps

A suspension of 4-chloro-3-nitrobenzenesulfonamide (1.664 g) triethylamine (2 mL) and 1-isopropylpiperidin-4-amine (1 g) in dioxane (10 mL) was stirred for 16 hours at 90° C. The reaction mixture was cooled to room temperature and the solid material was filtered off. The solid material was washed with 20% methanol/dichloromethane, and the mixture was dried under vacuum, to provide the product.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08557983B2
Source datasetuspto-grants-2013_10
ORD IDord-23849bd3acc1477fbbc8c236dfddb788
Source noteuspto-grants-2013_10