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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 334711Generated: October 30, 2026

2,6-Dimethoxybenzoyl chloride → 2,6-dimethoxy-N-methyl-N-(4-(pyridin-2-yl)but-3-ynyl)benzamide

https://huagongshe.com/reaction/334711

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2,6-Dimethoxybenzoyl chlorideHCID 74810—
ReactantDiisopropylethylamineHCID 81531—
ReactantN-methyl-4-(pyridin-2-yl)but-3-yn-1-amineHCID 66598286—
SolventChloroformHCID 6212—
Product2,6-dimethoxy-N-methyl-N-(4-(pyridin-2-yl)but-3-ynyl)benzamideHCID 6659830712%

Reaction Conditions

Temperature0 °C

Reaction Steps

2,6-Dimethoxy-benzoyl chloride (81 mg, 0.41 mmol) was added to a solution of methyl-(4-pyridin-2-yl-but-3-ynyl)-amine (50 mg, 0.31 mmol) and DIEA (69 μL, 0.41 mmol) in chloroform (2 mL) at 0° C. The reaction mixture was stirred at 0° C. for 10 min., at room temperature for 14 hours, quenched by the addition of water and extracted twice with chloroform. The organic phase was washed with saturated solution of NaHCO3, brine, dried over MgSO4, filtered and evaporated. The crude residue was purified by flash chromatography (DCM/MeOH 95:5) to yield 2,6-dimethoxy-N-methyl-N-(4-(pyridin-2-yl)but-3-ynyl)benzamide (12 mg, 37 μmol, 12%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08883826B2
Source datasetuspto-grants-2014_11
ORD IDord-ef1f302f3643489198ca291b16ddc360
Source noteuspto-grants-2014_11