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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1412329Generated: November 2, 2026

Pyridine → HCID 178438624, compound

https://huagongshe.com/reaction/1412329

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPyridineHCID 1049—
ReactantAcetic AnhydrideHCID 7918—
ReactantHCID 178438621HCID 178438621—
SolventEthyl AcetateHCID 8857—
ProductHCID 178438624HCID 17843862447%

Reaction Conditions

Temperature120 °C

Reaction Steps

A mixture of 4′-({4-[trans-4-(2-hydroxy-2-methylpropoxy)cyclohexyl]-2-methyl-5-oxo-7-propyl-4,5-dihydro[1,2,4]triazolo[1,5-a]pyrimidin-6-yl}methyl)biphenyl-2-carbonitrile (0.2 g), acetic anhydride (5 mL) and pyridine (5 mL) was stirred at 120° C. for 6 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. The obtained residue was purified by silica gel column chromatography to give the title compound as a colorless solid (0.1 g, 47%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08921379B2
Source datasetuspto-grants-2014_12
ORD IDord-223095bf0a0d4fa28f8db5b92c3b83cd
Source noteuspto-grants-2014_12