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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1189282Generated: October 30, 2026

4-Fluorobenzoyl chloride → 4-fluoro-N-methyl-N-(4-(pyridin-2-yl)but-3-ynyl)benzamide

https://huagongshe.com/reaction/1189282

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-Fluorobenzoyl chlorideHCID 67879—
ReactantN-methyl-4-(pyridin-2-yl)but-3-yn-1-amineHCID 66598286—
Product4-fluoro-N-methyl-N-(4-(pyridin-2-yl)but-3-ynyl)benzamideHCID 6659846758.8%

Reaction Steps

The title compound was prepared in accordance with the general method of Example 199(D), from N-methyl-4-(pyridin-2-yl)but-3-yn-1-amine (100 mg, 0.62 mmol) and 4-fluorobenzoyl chloride (99 mg, 0.62 mmol). The crude residue was purified over silicagel chromatography (prepacked 10 g silicagel column, DCM/MeOH:98/2 as eluent) to afford 103 mg of 4-fluoro-N-methyl-N-(4-(pyridin-2-yl)but-3-ynyl)benzamide as a brown oil (Yield: 58%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08674106B2
Source datasetuspto-grants-2014_03
ORD IDord-11fecf52951e457da8d9589b2b61711d
Source noteuspto-grants-2014_03