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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1801867Generated: October 31, 2026

Water → 4-(3-Chloro-4 (3-fluorobenzyloxy)phenylamino)-quinazoline-6-carboxylic acid methoxy methyl amide

https://huagongshe.com/reaction/1801867

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantTetrahydrofuranHCID 8028—
ReactantAmmonium ChlorideHCID 25517—
ReactantMethanamine, N-methoxy-, hydrochloride (1:1)HCID 81138—
Reactant4-(3-Chloro-4-(3-fluorobenzyloxy)phenylamino)-quinazoline-6-carboxylic acid methyl esterHCID 46928115—
Product4-(3-Chloro-4 (3-fluorobenzyloxy)phenylamino)-quinazoline-6-carboxylic acid methoxy methyl amideHCID 68748957—

Reaction Steps

In tetrahydrofuran (230 ml) was dissolved 4-(3-chloro-4-(3-fluorobenzyloxy)phenylamino)-quinazoline-6-carboxylic acid methyl ester (X-1, 11.6 g), N,O-dimethylhydroxylamine hydrochloride (7.8 g) was added, and 2 mol/L iPrMgCl tetrahydrofuran solution (79.8 ml) was added dropwise over 30 minutes under ice cooling. After completion of addition, the mixture was stirred for 20 minutes under ice cooling and, after completion of the reaction, 200 ml of aqueous saturated ammonium chloride solution was added. After 100 ml of water was added to the mixture, the mixture was extracted with ethyl acetate, and the organic layer was dried over sodium sulfate. The filtrate was concentrated to obtain 4-(3-chloro-4-(3-fluorobenzyloxy)phenylamino)-quinazoline-6-carboxylic acid methoxy methyl amide (XI-1, 12.7 g) as a pale yellow solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08349857B2
Source datasetuspto-grants-2013_01
ORD IDord-ab37c420b0b44f50a8d23767071adf7f
Source noteuspto-grants-2013_01