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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1699095Generated: November 1, 2026

Methanol → Ethyl (7-chloro-2,4-dioxo-3,4-dihydroquinazolin-1(2H)-yl)acetate

https://huagongshe.com/reaction/1699095

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanolHCID 887—
ReactantEthyl AcetateHCID 8857—
ReactantHexamethyldisilazaneHCID 13838—
Reactant7-Chloroquinazoline-2,4-diolHCID 246858—
CatalystSulfuric AcidHCID 1118—
SolventTolueneHCID 1140—
ProductEthyl (7-chloro-2,4-dioxo-3,4-dihydroquinazolin-1(2H)-yl)acetateHCID 9838691—

Reaction Steps

To a mixed suspension of 7-chloro-2,4-dioxo-1,2,3,4-tetrahydroquinazoline (20 g) and hexamethyldisilazane (16.42 g) in toluene (60 ml) was added sulfuric acid (0.80 g) dropwise and the silylation reaction was carried out at an internal temperature of 110˜120° C. for 6 hours. After completion of silylation, the toluene was distilled off to recover a concentrate containing 7-chloro-2,4-bis(trimethylsilyloxy)quinazoline. To this concentrate were added propylene carbonate (40 ml), ethyl chloroacetate (13.72 g) and ethyl bromoacetate (3.40 g), and the reaction was carried out at an internal temperature of 125˜140° C. for 6 hours. After completion of reaction, the reaction mixture was cooled to an internal temperature of ≦70° C. and ethyl acetate (80 ml) was added. Then, methanol (60 ml) was added dropwise over 30 minuets. After completion of dropwise addition, the mixture was cooled to ≦20° C. and stirred for 1 hour. The resulting crystal crop was harvested by filtration, washed serially with methanol (40 ml) and water (100 ml) and dried to provide ethyl 2-(7-chloro-2,4-dioxo-1,2,3,4-tetrahydroquinazolin-1-yl)acetate (28.16 g) as white crystals.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06344559B1
Source datasetuspto-grants-2002_02
ORD IDord-b1819d7d97f4490cb77baca645d139da
Source noteuspto-grants-2002_02