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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 659958Generated: November 1, 2026

p-Toluenesulfonic acid → HCID 86643500, compound

https://huagongshe.com/reaction/659958

Reaction equation

Participants

RoleNameHCIDCharge
Reactantp-Toluenesulfonic acidHCID 6101—
Reactant2-Chloro-3-pyridylamineHCID 80528—
ReactantToluene waterHCID 22272177—
ReactantHCID 68430510HCID 68430510—
SolventTolueneHCID 1140—
SolventEthyl acetate hexaneHCID 21226206—
ProductHCID 86643500HCID 8664350049.8%

Reaction Steps

A mixture of p-toluenesulfonic acid (10 mg), 2-(4-Fluoro-phenyl)-1-(2-methylthio-pyrimidin-4-yl)-ethanone (200 mg, 0.76 mmoles) and 3-amino-2-chloropyridine (90 mg, 0.7 mmoles) in 3 mL of toluene was refluxed overnight with a Dean-Stark removal of water/toluene azeotrope. The reaction mixture was further concentrated, the brown residue suspended in an ethyl acetate/hexane mixture (9/1) and filtered. The solid was solubilised in ethyl acetate and purified by chromatography on silica gel (ethylacetate/hexane 1/1) to give 130 mg of (2-Chloro-pyridin-3-yl)-[2-(4-fluoro-phenyl)-1-(2-methylthio-pyrimidin-4-yl)-ethylidene]-amine as a brown oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08084395B2
Source datasetuspto-grants-2011_12
ORD IDord-a07094c3b3514f33a195038242b7295b
Source noteuspto-grants-2011_12