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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1294174Generated: November 2, 2026

Dimethylformamide → 2-[4-[(5-Methyl-2-phenyl-4-thiazolyl)methoxy]benzyloxy]nicotinonitrile

https://huagongshe.com/reaction/1294174

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethylformamideHCID 6228—
ReactantSodium hydrideHCID 24758—
Reactant2-ChloronicotinonitrileHCID 81079—
Reactant4-(5-Methyl-2-phenyl-4-thiazolylmethoxy)benzyl alcoholHCID 68886269—
SolventWaterHCID 962—
Product2-[4-[(5-Methyl-2-phenyl-4-thiazolyl)methoxy]benzyloxy]nicotinonitrileHCID 6888591577%

Reaction Steps

To admixture of [4-[(5-methyl-2-phenyl-4-thiazolyl)methoxy]phenyl]methanol (4.50 g), 2-chloro-3-cyanopyridine (1.91 g) and N,N-dimethylformamide (50 mL) was added sodium hydride (60%, oil, 0.66 g) under ice-cooling. The reaction mixture was stirred at room temperature for 3 hrs. Water was added to the reaction mixture and the mixture was extracted with ethyl acetate. The organic layer was washed with saturated brine, dried over anhydrous magnesium sulfate, and concentrated. The obtained residue was subjected to silica gel column chromatography to give crystals (4.38 g, 77%) of 2-[4-[(5-methyl-2-phenyl-4-thiazolyl)methoxy]benzyloxy]nicotinonitrile from a fraction eluted with ethyl acetate-hexane (1:3, v/v). Recrystallization from ethyl acetate-hexane gave colorless prism crystals. melting point: 120-121° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07238716B2
Source datasetuspto-grants-2007_07
ORD IDord-5f38dbb38a3b4e15bc798d55bf17bb2b
Source noteuspto-grants-2007_07