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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1616135Generated: November 1, 2026

4-Chlorobenzylamine → HCID 67281627, compound

https://huagongshe.com/reaction/1616135

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-ChlorobenzylamineHCID 66036—
ReactantDiisopropylethylamineHCID 81531—
ReactantHCID 67282899HCID 67282899—
SolventIsopropanolHCID 3776—
ProductHCID 67281627HCID 6728162775%

Reaction Conditions

Temperature100 °C

Reaction Steps

To a suspension of methyl 3-benzyl-2-chloro-4-oxo-3,4-dihydroquinazoline-7-carboxylate (0.20 g, 0.37 mmol) in isopropyl alcohol (4 mL) was added N,N-diisopropylethylamine (0.13 mL, 0.77 mmol) and p-chlorobenzylamine (0.11 mL, 0.91 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 80% EtOAc/hexanes) to afford methyl 3-benzyl-2-[(4-chlorobenzyl)amino]-4-oxo-3,4-dihydroquinazoline-7-carboxylate (0.12 g, 75%). LC-MS: (FA) ES+434.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08765773B2
Source datasetuspto-grants-2014_07
ORD IDord-3ae136f6f55a433dbf844bc9cbc6f8bb
Source noteuspto-grants-2014_07