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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 513805Generated: October 31, 2026

Ammonium formate → 2-amino-N-(4-methoxy-quinolin-8-yl)benzenesulfonamide

https://huagongshe.com/reaction/513805

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAmmonium formateHCID 2723923—
Reactant2-Amino-N-(7-chloro-4-methoxy-quinolin-8-yl)-benzenesulfonamideHCID 68183053—
CatalystPalladiumHCID 23938—
SolventAcetic AcidHCID 176—
Product2-amino-N-(4-methoxy-quinolin-8-yl)benzenesulfonamideHCID 6818299032.2%

Reaction Conditions

Temperature70 °C

Reaction Steps

10% Pd—C (97 mg) was added to a solution of 2-amino-N-(7-chloro-4-methoxy-quinolin-8-yl)-benzenesulfonamide 570 (470 mg, 1.8 mmol), ammonium formate (571 mg, 9.2 mmol) in 50% AcOH (10 ml) and the mixture was heated to 70° C. for 15 h. After cooling, the solvent was removed in vacuo. The residue was dissolved in EtOAc (100 ml) and the organic phase was washed with sat. NaHCO3 solution (50 ml), dried (MgSO4) concentrated in vacuo. The crude residue was purified by column chromatography DCM/MeOH (99:1) as the eluent to give the title compound (191 mg, 32%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09102688B2
Source datasetuspto-grants-2015_08
ORD IDord-a01f488307ec41a694405a51936e1d49
Source noteuspto-grants-2015_08