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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 599362Generated: October 30, 2026

4-Chloroaniline → N-(4-Chlorophenyl)-2-(quinolin-4-ylmethylthio)pyridine-3-carboxamide

https://huagongshe.com/reaction/599362

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-ChloroanilineHCID 7812—
ReactantEthyl AcetateHCID 8857—
ReactantDiisopropylethylamineHCID 81531—
Reactant2-(Quinolin-4-ylmethylthio)pyridine-3-carboxylic acidHCID 67053953—
SolventDimethylformamideHCID 6228—
ProductN-(4-Chlorophenyl)-2-(quinolin-4-ylmethylthio)pyridine-3-carboxamideHCID 1164713475%

Reaction Steps

O-(7-Azabenzotriazol-1-yl)-N,N,N′,N′-tetrauroniumhexafluorophosphate (140 mg, 0.38 mmol) was added to a solution of 2-(quinolin-4-ylmethylthio)pyridine-3-carboxylic acid (Reference Compound No. 7-1.91 mg, 0.31 mmol), 4-chloroaniline (52 mg, 0.40 mmol) and N,N-diisopropylethylamine (0.13 mL, 0.74 mmol) in anhydrous N,N-dimethylformamide (2.0 mL) at room temperature, and the mixture was stirred for 24 hours. Ethyl acetate (50 mL) was added thereto, and the whole was washed with saturated aqueous sodium hydrogencarbonate solution (50 mL, twice) and brine (50 mL), The organic layer was dried over anhydrous magnesium sulfate. The solvent was evaporated under reduced pressure, and then the precipitated solid was filtered off and washed with a mixture of diethyl ether and ethyl acetate (1:1). The resulting solid was dried at 50° C. under reduced pressure to give 93 mg of the target compound as a reddish-brown solid (Yield: 75%)

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07897774B2
Source datasetuspto-grants-2011_03
ORD IDord-3bd7756da98d44058aadb589a1dc0187
Source noteuspto-grants-2011_03