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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 472737Generated: October 31, 2026

Water → Cyclobutanecarboxylic acid (2-{1-[(5-chloro-2,4-dimethoxy-phenylcarbamoyl)-methyl]-2,4-dioxo-1,4-dihydro-2H-quinazolin-3-yl}-ethyl)-amide

https://huagongshe.com/reaction/472737

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantEthyl AcetateHCID 8857—
ReactantCyclobutanecarbonyl chlorideHCID 78705—
Reactant2-[3-(2-Amino-ethyl)-2,4-dioxo-3,4-dihydro-2H-quinazolin-1-yl]-N-(5-chloro-2,4-dimethoxy-phenyl)-acetamide trifluoroacetateHCID 68588503—
SolventTetrahydrofuranHCID 8028—
SolventTriethylamineHCID 8471—
ProductCyclobutanecarboxylic acid (2-{1-[(5-chloro-2,4-dimethoxy-phenylcarbamoyl)-methyl]-2,4-dioxo-1,4-dihydro-2H-quinazolin-3-yl}-ethyl)-amideHCID 59317680—

Reaction Steps

To a suspension of 2-[3-(2-Amino-ethyl)-2,4-dioxo-3,4-dihydro-2H-quinazolin-1-yl]-N-(5-chloro-2,4-dimethoxy-phenyl)-acetamide trifluoroacetate (75 mg, 0.17 mmol) in THF (1 ml), triethylamine is added (0.06 ml, 0.43 mmol) followed cyclobutane carbonyl chloride (30 mg, 0.26 mmol). The mixture is stirred overnight at RT. Water (3 ml) and then EtOAc is added to the mixture to give a suspension which is filtered to remove the solid. The filtrate is washed with water, dried and evaporated to afford the title compound, [M+H]+ 515

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08633211B2
Source datasetuspto-grants-2014_01
ORD IDord-90b9e20ac8b6461ebaf911cee712faf7
Source noteuspto-grants-2014_01