Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1061549Generated: November 1, 2026

4-chloro-3-nitro-N-(pyridin-3-ylmethyl)benzenesulfonamide → 4-Amino-3-nitro-N-(3-pyridinylmethyl)benzenesulfonamide

https://huagongshe.com/reaction/1061549

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-chloro-3-nitro-N-(pyridin-3-ylmethyl)benzenesulfonamideHCID 2858305—
ReactantAmmonia methanolHCID 21705897—
Product4-Amino-3-nitro-N-(3-pyridinylmethyl)benzenesulfonamideHCID 22285168—

Reaction Conditions

Temperature100 °C

Reaction Steps

Into a saturated ammonia-methanol solution (60 ml) was added 4-chloro-3-nitro-N-(pyridin-3-ylmethyl)benzenesulfonamide (2.77 g), followed by about 2 days of heating at 100° C. in a sealed tube. After the reaction, the solvent was evaporated under reduced pressure and the formed yellow crystals were collected by filtration and dried to obtain 4-amino-3-nitro-N-(pyridin-3-ylmethyl)benzenesulfonamide (2.51 g). Hereinafter, the compound of Reference Examples 26 was obtained similarly.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06960591B2
Source datasetuspto-grants-2005_11
ORD IDord-9f9472e3325a4e56940e70a7170ae712
Source noteuspto-grants-2005_11