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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1616116Generated: November 1, 2026

4-Chlorobenzylamine → HCID 67282640, compound

https://huagongshe.com/reaction/1616116

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-ChlorobenzylamineHCID 66036—
ReactantDiisopropylethylamineHCID 81531—
ReactantHCID 67282409HCID 67282409—
SolventIsopropanolHCID 3776—
ProductHCID 67282640HCID 6728264093%

Reaction Conditions

Temperature100 °C

Reaction Steps

To a suspension of methyl 2-chloro-3-methyl-4-oxo-3,4-dihydroquinazoline-7-carboxylate (70.0 mg, 0.28 mmol) in isopropyl alcohol (3 mL) was added N,N-diisopropylethylamine (0.10 mL, 0.58 mmol) and p-chlorobenzylamine (84.2 μL, 0.69 mmol). The reaction mixture was heated to 100° C. and stirred for 1 h. The mixture was then cooled to rt and concentrated. The residue was purified by flash silica gel chromatography (0% to 5% MeOH/DCM) to afford methyl 2-[(4-chlorobenzyl)amino]-3-methyl-4-oxo-3,4-dihydroquinazoline-7-carboxylate (92 mg, 93%). LC-MS: (FA) ES+ 358.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08765773B2
Source datasetuspto-grants-2014_07
ORD IDord-96475c9dfb6b4707b0b8eccc8b07a386
Source noteuspto-grants-2014_07