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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 519561Generated: October 30, 2026

Pyridine → HCID 178438565, compound

https://huagongshe.com/reaction/519561

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPyridineHCID 1049—
Reactant4-Toluenesulfonyl chlorideHCID 7397—
ReactantHCID 178438573HCID 178438573—
SolventEthyl AcetateHCID 8857—
ProductHCID 178438565HCID 17843856585%

Reaction Conditions

Temperature110 °C

Reaction Steps

A mixture of trans-N′-acetyl-4-{6-[(2′-cyanobiphenyl-4-yl)methyl]-5-oxo-7-propyl[1,2,4]triazolo[1,5-a]pyrimidin-4(5H)-yl}cyclohexanecarbohydrazide (0.4 g), p-toluenesulfonyl chloride (0.42 g) and pyridine (10 mL) was stirred at 110° C. for 5 hr. The reaction mixture was diluted with ethyl acetate, washed with 1 N hydrochloric acid and then with saturated brine, and dried over anhydrous magnesium sulfate. The solvent was evaporated under reduced pressure and the residue was purified by silica gel column chromatography to give the title compound as a colorless solid (0.33 g, 85%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09115136B2
Source datasetuspto-grants-2015_08
ORD IDord-6fb019d4bd7a4f758c0735e48f80ecc5
Source noteuspto-grants-2015_08