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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1189278Generated: November 2, 2026

m-Anisoyl chloride → 3-methoxy-N-methyl-N-(4-(pyridin-2-yl)but-3-ynyl)benzamide

https://huagongshe.com/reaction/1189278

Reaction equation

Participants

RoleNameHCIDCharge
Reactantm-Anisoyl chlorideHCID 74374—
ReactantDiisopropylethylamineHCID 81531—
ReactantN-methyl-4-(pyridin-2-yl)but-3-yn-1-amineHCID 66598286—
SolventDichloromethaneHCID 6344—
Product3-methoxy-N-methyl-N-(4-(pyridin-2-yl)but-3-ynyl)benzamideHCID 6659826963.6%

Reaction Steps

N-Methyl-4-(pyridin-2-yl)but-3-yn-1-amine (50 mg, 0.31 mmol) was dissolved in DCM (2 mL) and DIEA (67 μl, 0.41 mmol) was added at room temperature. The resulting mixture was cooled to 0° C. before the addition of 3-methoxybenzoyl chloride (69 mg, 0.41 mmol). After stirring overnight at room temperature, the mixture was quenched with water and extracted with DCM. DCM fractions were washed with water (10 mL), NaHCO3 sat (2*10 mL), water (10 mL), brine (10 mL). The solvent was removed and the crude residue was purified over silicagel chromatography (prepacked 10 g silicagel column, DCM/MeOH: from 100/0 to 95/5 as eluent) to afford 58 mg of 3-methoxy-N-methyl-N-(4-(pyridin-2-yl)but-3-ynyl)benzamide (Yield: 63%) as a brown oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08674106B2
Source datasetuspto-grants-2014_03
ORD IDord-64e7487d2a7f44019e35629ae65d1995
Source noteuspto-grants-2014_03