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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 33943Generated: October 26, 2026

Isonicotinic Acid → N-(4-methoxyphenyl)pyridine-4-carboxamide

https://huagongshe.com/reaction/33943

Reaction equation

Participants

RoleNameHCIDCharge
ReactantIsonicotinic AcidHCID 5922—
ReactantP-AnisidineHCID 7732—
ReactantTriethylamineHCID 8471—
ReactantPropylphosphonic anhydrideHCID 111923—
SolventEthyl AcetateHCID 8857—
ProductN-(4-methoxyphenyl)pyridine-4-carboxamideHCID 53220788%

Reaction Conditions

Temperature23 °C

Reaction Steps

A solution of p-anisidine (2.46 g, 20 mmol) and triethylamine (13.9 mL, 100 mmol) in ethyl acetate (200 mL) was treated with isonicotinic acid (2.46 g, 20 mmol) followed by 1-propanephosphonic acid cyclic anhydride (50% in ethyl acetate, 15.1 mL, 24 mmol). After stirring at 23° C. for 4 h, the reaction mixture was diluted with ethyl acetate, was washed with water and with brine, and the organic layer was dried (MgSO4), was filtered, and was concentrated in vacuo. Purification by silica gel chromatography with chloroform-methanol (40:1) gave 4 g (88% yield) of the title compound; diagnostic 13C NMR signals (100 MHz, CD3OD/CDCl3) δ 164.825, 157.213, 149.758, 143.349, 130.989, 123.085, 122.068, 55.285; MS (AP/Cl) 229.3 (M+H)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07429665B2
Source datasetuspto-grants-2008_09
ORD IDord-1d9c6cc5ff654151b13c4dd5eca8c035
Source noteuspto-grants-2008_09