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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1250490Generated: October 31, 2026

M-Cresol → N-(4-methylphenyl)-4-methoxy-6-(3-methylphenoxy)-2-pyridine carboxamide

https://huagongshe.com/reaction/1250490

Reaction equation

Participants

RoleNameHCIDCharge
ReactantM-CresolHCID 342—
ReactantSodium hydrideHCID 24758—
ReactantN-(4-methylphenyl)-6-bromo-4-methoxy-2-pyridine carboxamideHCID 18326207—
CatalystCupric ChlorideHCID 24014—
SolventDimethylformamideHCID 6228—
SolventHexaneHCID 8058—
ProductN-(4-methylphenyl)-4-methoxy-6-(3-methylphenoxy)-2-pyridine carboxamideHCID 15906600—

Reaction Conditions

Temperature100 °C

Reaction Steps

0.45 g (0.0019×2.2 mol) of 3-methyl phenol was dissolved in about 10 ml of DMF. The obtained solution was further mixed with 0.15 g (ca. 60% in mineral oil; 0.0019×2.0 mol) of NaH and then with 0.60 g (0.0019 mol) of N-(4-methylphenyl)-6-bromo-4-methoxy-2-pyridine carboxamide. After adding 0.19 g (0.0019×1.0 mol) of copper chloride (I), the solution was stirred at about 100° C. for about 4 hours, and then allowed to stand for cooling to room temperature. After the reaction solution was distributed in hexane-saturated sodium bicarbonate water, the organic phase of the solution was washed with saturated brine and dried with anhydrous sodium sulfate, followed by concentration thereof. Thereafter, the concentrated solution was purified by silica gel column chromatography (eluting solution: ethyl acetate/hexane), thereby obtaining an aimed product.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06339045B1
Source datasetuspto-grants-2002_01
ORD IDord-4e8cf4c5f1fb4848b7d607c7c9bd8232
Source noteuspto-grants-2002_01