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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 8721Generated: October 23, 2026

Diisopropylethylamine → 2-(1-benzyl-1,4,6,7-tetrahydro-imidazo[4,5-c]pyridin-5-yl)-6,7-dimethoxy-3H-quinazolin-4-one

https://huagongshe.com/en/reaction/8721

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiisopropylethylamineHCID 81531—
Reactant1-Benzyl-1,4,6,7-tetrahydro-imidazo[4,5-c]pyridine dihydrochlorideHCID 21983657—
Reactant2-Chloro-6,7-dimethoxy-3H-quinazolin-4-oneHCID 135456664—
SolventWaterHCID 962—
Solvent2-MethoxyethanolHCID 8019—
Product2-(1-benzyl-1,4,6,7-tetrahydro-imidazo[4,5-c]pyridin-5-yl)-6,7-dimethoxy-3H-quinazolin-4-oneHCID 13572350829.9%

Reaction Conditions

Temperature120 °C

Reaction Steps

A mixture of 2-chloro-6,7-dimethoxy-3H-quinazolin-4-one 1 (wherein R is methyl and Z is —C(O)—, 296 mg, 1.24 mmol), 1-benzyl-1,4,6,7-tetrahydro-imidazo[4,5-c]pyridine dihydrochloride 15a (440 mg, 1.54 mmol)) and diisopropylethylamine (1.2 g, 9.26 mmol) in 2-methoxyethanol (10 mL) was stirred at 120° C. for 6 hours. The reaction mixture was concentrated in vacuo to give an oil residue, which was diluted with water. The white precipitate that formed was collected by filtration to give 155 mg of 2-(1-benzyl-1,4,6,7-tetrahydro-imidazo[4,5-c]pyridin-5-yl)-6,7-dimethoxy-3H-quinazolin-4-one 501, [M+H]+=418.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07091200B2
Source datasetuspto-grants-2006_08
ORD IDord-1072292ad8ec44c99727818e337ae56f
Source noteuspto-grants-2006_08