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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2415133Generated: October 31, 2026

Ammonium Chloride → 3-(4-Methoxy-quinolin-2-ylamino)-2-methyl-propionamide

https://huagongshe.com/reaction/2415133

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAmmonium ChlorideHCID 25517—
ReactantTrimethylaluminumHCID 16682925—
Reactant3-(4-Methoxy-quinolin-2-ylamino)-2-methyl-propionic acid methyl esterHCID 69837131—
SolventTolueneHCID 1140—
SolventDichloromethaneHCID 6344—
Product3-(4-Methoxy-quinolin-2-ylamino)-2-methyl-propionamideHCID 2264073048%

Reaction Steps

A slurry of ammonium chloride (0.38 g, 7.11 mmol) in dry methylene chloride (20 mL) at 0° C. was treated with trimethylaluminum (1 eq, 7.11 mmol, 3.6 mL of a 2M solution in toluene). The mixture was allowed to warm to room temperature over a period of two hours, at which time a solution of 3-(4-methoxy-quinolin-2-ylamino)-2-methyl-propionic acid methyl ester (0.33 eq, 2.37 mmol, 0.65 g) in dry methylene chloride (5 mL) was added. The solution stirred at room temperature for two hours, then was quenched slowly by addition of concentrated HCl (1 mL). After stirring for an additional 30 minutes, the mixture was diluted with 10% NaOH (30 mL) and brine (20 mL) and extracted into methylene chloride. The organic extracts were dried over Na2SO4, filtered and concentrated to an oil. Purification via column chromatography on silica (95:5 methylene chloride/methanolic ammonia) provided the product (0.29 g, 48%) as a white solid. [M+H]+ 260.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06818655B2
Source datasetuspto-grants-2004_11
ORD IDord-400a4decbdeb4e878363679ae45d5039
Source noteuspto-grants-2004_11