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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1846335Generated: November 1, 2026

p-Toluenesulfonic acid → HCID 46841411, compound

https://huagongshe.com/reaction/1846335

Reaction equation

Participants

RoleNameHCIDCharge
Reactantp-Toluenesulfonic acidHCID 6101—
Reactant2-amino-N-(4-chlorophenyl)benzamideHCID 670472—
Reactant6-Chloropyridine-3-carbaldehydeHCID 2764053—
ReactantSodium BisulfiteHCID 23665763—
SolventEthyl AcetateHCID 8857—
SolventDimethylacetamideHCID 31374—
ProductHCID 46841411HCID 468414114%

Reaction Conditions

Temperature150 °C

Reaction Steps

2-Amino-N-(4-chlorophenyl)benzamide (0.500 g, 2.03 mmol) and 6-chloronicotinaldehyde (2.23 mmol), NaHSO3 (0.253 g, 2.44 mmol) and p-TsOH (0.039 g, 0.20 mmol) were dissolved in DMA (20 mL) and heated at 150° C. for 21 hours. The mixture was cooled to room temperature, diluted with ethyl acetate (100 mL), washed with water (2×200 mL), dried (Na2SO4), filtered, and concentrated. Flash chromatograph on silica gel, eluting with 30% ethyl acetate/heptane to 70% ethyl acetate/heptane, afforded the title compound as a white solid (4%). 1H-NMR (300 MHz, DMSO-6): δ 8.46 (d, J=2.1 Hz, 1H), 8.23 (d, J=8.1 Hz, 1H), 7.92-7.97 (m, 1H), 7.80-7.86 (m, 2H), 7.63-7.68 (m, 1H), 7.47-7.50 (m, 5H). MS (APCI) m/z: 368 (M+H)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08952021B2
Source datasetuspto-grants-2015_02
ORD IDord-0332d946e87041bcabe31fb53b986635
Source noteuspto-grants-2015_02