Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2058183Generated: October 26, 2026

Hydrochloric Acid → 2-Allylamino-6-methylnicotinic acid methyl ester

https://huagongshe.com/reaction/2058183

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantAllylamineHCID 7853—
ReactantSodium CarbonateHCID 10340—
ReactantMethyl 2-chloro-6-methylpyridine-3-carboxylateHCID 13055804—
CatalystDiethyl EtherHCID 3283—
SolventEthanolHCID 702—
Product2-Allylamino-6-methylnicotinic acid methyl esterHCID 12818656—

Reaction Steps

A stirred mixture of 9.25 g. (0.05 mole) of methyl 2-chloro-6-methylnicotinate, 2,85 g. (0.05 mole) of allylamine and 5.3 g. (0.05 mole) of sodium carbonate in 50 ml. of ethanol was heated under reflux for 5 hours. The mixture was filtered and the filtrate was evaporated in a rotary evaporator. The residue was diluted with 50 ml. of water and was extracted with 50 ml. of diethyl ether. The ether layer was dried over magnesium sulfate, filtered and was evaporated. The residue was passed through a neutral aluminum oxide column using ethyl acetate as the eluent. Evaporation of the ethyl acetate gave 3.1 g. of product. A small amount of this oil was dissolved in diethyl ether containing a few drops of ethanol and this solution was acidified with an ethereal hydrochloric acid solution. The precipitate which formed was collected and was recrystallized from ethyl acetate to give 2-allylamino-6-methylnicotinic acid methyl ester, m.p. 140°-2° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04215123
Source datasetuspto-grants-1980_07
ORD IDord-810224417b354735ba82b7500626e8b1
Source noteuspto-grants-1980_07