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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 388465Generated: October 30, 2026

Water → 3-[1-(4,6-Dimethyl-1,2-benzisothiazol-3-ylmethyl)-2,4-dioxo-1,4-dihydro-2H-quinazolin-3-yl]-pentanoic acid methyl ester

https://huagongshe.com/reaction/388465

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantPotassium CarbonateHCID 11430—
Reactant3-Bromomethyl-4,6-dimethyl-benzo[d]isothiazoleHCID 58497391—
Reactant3-(2,4-dioxo-1,4-dihydro-2H-quinazolin-3-yl)-pentanoic acid methyl esterHCID 68726363—
SolventDimethylformamideHCID 6228—
Product3-[1-(4,6-Dimethyl-1,2-benzisothiazol-3-ylmethyl)-2,4-dioxo-1,4-dihydro-2H-quinazolin-3-yl]-pentanoic acid methyl esterHCID 6874840780%

Reaction Conditions

Temperature100 °C

Reaction Steps

To a solution of 3-(2,4-dioxo-1,4-dihydro-2H-quinazolin-3-yl)-pentanoic acid methyl ester (50 mg, 0.18 mmol) (prepared according to example 2, steps 1-2) in DMF (10 mL) are added 3-bromomethyl-4,6-dimethyl-1,2-benzisothiazole (70 mg, 0.271 mmol) and K2CO3 (50 mg, 0.36 mmol) at room temperature under a nitrogen atmosphere. The solution is heated at 100° C. for 2 hours. The solution is cooled down and water is added. The solution is extracted with EtOAc and the combined organic layer is dried with MgSO4. The solution is filtered and the filtrate is concentrated. The residue is purified by flash chromatography with 20% EtOAc in Hexane as the eluent to afford 3-[1-(4,6-Dimethyl-1,2-benzisothiazol-3-ylmethyl)-2,4-dioxo-1,4-dihydro-2H-quinazolin-3-yl]-pentanoic acid methyl ester (65 mg, 80%) as a colorless foam.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08377949B2
Source datasetuspto-grants-2013_02
ORD IDord-d9ec5a36e5a14c9c9e2380e8bab494b7
Source noteuspto-grants-2013_02