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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1780581Generated: October 31, 2026

Pyridine → 2-methyl-N-[4-methyl-2-[2-(methylthio)-4-pyrimidinyl]phenyl]propanamide

https://huagongshe.com/reaction/1780581

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPyridineHCID 1049—
ReactantDiethyl EtherHCID 3283—
ReactantIsovaleryl chlorideHCID 66054—
Reactant4-Methyl-2-[2-(methylthio)-4-pyrimidinyl]benzenamineHCID 19047037—
SolventChloroformHCID 6212—
Product2-methyl-N-[4-methyl-2-[2-(methylthio)-4-pyrimidinyl]phenyl]propanamideHCID 19047033—

Reaction Steps

A solution of 11.7 g (0.11 mol) isovaleryl chloride in 15 mL dry chloroform was added dropwise with stirring to a solution of 23.1 g (0.10 mol) 4-methyl-2-[2-(methylthio)-4-pyrimidinyl]benzenamine and 12 g pyridine in 60 mL dry chloroform. Stirring was continued for 1 h at room temperature, after which the reaction mixture was diluted with 200 mL ether and washed successively with water, 0.5N hydrochloric acid solution, and brine. The organic extracts were dried over magnesium sulfate, filtered, and evaporated to dryness. The crude product was purified by chromatography on silica gel using 10:1 chlorobutane/ethyl acetate mixture as eluent to yield 28.3 g of the title compound as white crystals melting at 134°-135° C. 1H NMR (CDCl3): δ 1.23 (d,6H), 2.30 (s,3H), 2.40 (s,3H) 2.47 (m,1H), 7.40-8.6 (5H), 10.7(s,1H,NH).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05631206
Source datasetuspto-grants-1997_05
ORD IDord-11d55361f24242fdb56899436bd16639
Source noteuspto-grants-1997_05