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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1417283Generated: October 25, 2026

Methane → N-[4-(3-amino-phenyl)-thiazol-2-yl]-4-methyl-benzenesulfonamide

https://huagongshe.com/reaction/1417283

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethaneHCID 297—
Reactant4-Methyl-N-[4-(3-nitro-phenyl)-thiazol-2-yl]-benzenesulfonamideHCID 4233969—
CatalystPalladiumHCID 23938—
SolventMethanolHCID 887—
SolventEthyl AcetateHCID 8857—
ProductN-[4-(3-amino-phenyl)-thiazol-2-yl]-4-methyl-benzenesulfonamideHCID 2184556779.7%

Reaction Steps

A solution of 1.5 g of 4-methyl-N-[4-(3-nitro-phenyl)-thiazol-2-yl]-benzenesulfonamide in 150 ml of methanol and 70 ml of ethyl acetate was hydrogenated at room temperature after the addition of 0.15 g of palladium on active charcoal (10%). The catalyst was filtered off and the filtrate was concentrated. Crystallization from ethyl acetate/hexane (1:1) yielded 1.1 g of N-[4-(3-amino-phenyl)-thiazol-2-yl]-4-methyl-benzenesulfonamide as a colorless solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05877193
Source datasetuspto-grants-1999_03
ORD IDord-4e3219a023054055b13884b71cf78be1
Source noteuspto-grants-1999_03