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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 235261Generated: October 26, 2026

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

https://huagongshe.com/reaction/235261

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethylamineHCID 6329—
Reactant4-(Pyridin-3-yl)but-3-yn-1-olHCID 10582917—
SolventWaterHCID 962—
ProductN-methyl-4-(pyridin-3-yl)but-3-yn-1-amineHCID 15860335546.1%

Reaction Steps

An aqueous methylamine solution (5mL, 40%, 58.7 mmole) was mixed with XII (200 mg, 0.08 mmole) and stirred for 3 hr. in a sealed tube at 45° C. After the reaction was complete, water (10 mL) was added to the cooled reaction mixture, and the reaction mixture was extracted with chloroform (10×5 mL). The combined organic extracts were dried over anhydrous sodium sulfate, filtered and concentrated The residue obtained was chromatographed on a silica gel column using methanol:chloroform (1:9) and then with a chloroform: methanol mixture containing 1% triethylamine as eluent. About 70 mg of XIII was obtained as a slightly yellow syrup, which was distilled at 110°-112° C., 0.04 mm Hg. XIII was converted to its mono fumarate salt form, which exhibits a melting point of 103°-104° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05597919
Source datasetuspto-grants-1997_01
ORD IDord-cd177f4c4c464ae489b8a855b8edc21c
Source noteuspto-grants-1997_01