Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 422464Generated: October 31, 2026

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

https://huagongshe.com/reaction/422464

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 numberUS08101637B2
Source datasetuspto-grants-2012_01
ORD IDord-ee5ca62c43804095b05baaa1e9f513ec
Source noteuspto-grants-2012_01