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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 220122Generated: October 28, 2026

Triethylamine → 4-Chloroquinazoline-6-carboxylic acid methoxymethylamide

https://huagongshe.com/reaction/220122

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantPhosphorus oxychlorideHCID 24813—
ReactantSodium BicarbonateHCID 516892—
ReactantHCID 178496796HCID 178496796—
SolventTolueneHCID 1140—
SolventEthyl AcetateHCID 8857—
Product4-Chloroquinazoline-6-carboxylic acid methoxymethylamideHCID 86630923—

Reaction Conditions

Temperature130 °C

Reaction Steps

4-Hydroxyquinazoline-6-carboxylic acid methoxymethylamide (XIII-1, 2.9 g) was suspended in toluene (57 ml), and 6.8 ml of triethylamine and 3.4 ml of phosphorus oxychloride were added, followed by stirring at 130° C. for 30 minutes. After completion of the reaction, the reaction mixture was cooled to room temperature, and 50 ml of aqueous saturated sodium bicarbonate solution and ethyl acetate were added. Sodium bicarbonate was added until the aqueous layer exhibited a pH 8, followed by extraction with ethyl acetate. The organic layer was washed with aqueous saturated sodium bicarbonate solution, dried over sodium sulfate. After concentration, the crystalline residue was washed with diethyl ether, and dried to obtain 4-chloroquinazoline-6-carboxylic acid methoxymethylamide (XIV-1, 2.3 g) as a white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08202879B2
Source datasetuspto-grants-2012_06
ORD IDord-6fe4313276964d158ebaf1f746689949
Source noteuspto-grants-2012_06