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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 334751Generated: October 28, 2026

Methylamine → N-methyl-4-(pyridin-2-yl)but-3-yn-1-amine

https://huagongshe.com/reaction/334751

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethylamineHCID 6329—
Reactant4-(Pyridin-2-yl)but-3-ynyl methanesulfonateHCID 86630252—
ProductN-methyl-4-(pyridin-2-yl)but-3-yn-1-amineHCID 6659828639%

Reaction Conditions

Temperature45 °C

Reaction Steps

4-(Pyridin-2-yl)but-3-ynyl methanesulfonate (2.90 g, 12.87 mmol) was dissolved in methylamine 40% in aqueous solution (20 mL) and stirred for 3 hours under nitrogen at 45° C. The reaction mixture was cooled with ice, quenched with water and extracted with DCM. The organic phases were washed with brine, dried over MgSO4 and concentrated. The crude residue was purified over silicagel chromatography (prepacked 70 g silicagel column, DCM/MeOH: from 90/10 to 90/10 with 1% of TEA as eluent) to afford 817 mg N-methyl-4-(pyridin-2-yl)but-3-yn-1-amine (Yield: 39%) as a brown oil

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08883826B2
Source datasetuspto-grants-2014_11
ORD IDord-cad64ee4a0524c85a4b2b7bc62bf7c84
Source noteuspto-grants-2014_11