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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 67082Generated: October 29, 2026

Triethylamine → 1-benzyl-4-(1,2,3,4-tetrahydro-2-oxo-3-quinazolinyl)piperidine

https://huagongshe.com/reaction/67082

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
Reactant1,1'-CarbonyldiimidazoleHCID 68263—
Reactant1-Benzyl-4-[N-(o-aminobenzyl)-amino]-piperidine trihydrochlorideHCID 20497164—
SolventAcetonitrileHCID 6342—
Product1-benzyl-4-(1,2,3,4-tetrahydro-2-oxo-3-quinazolinyl)piperidineHCID 1305102154.6%

Reaction Steps

In this reference example, 4.04 g of 1-benzyl-4-[N-(o-aminobenzyl)-amino]-piperidine trihydrochloride, 3.04 g of triethylamine, 2.03 g of 1,1'-carbonyldiimidazole and 50 ml of acetonitrile are mixed and stirred at room temperature for 4 hours. Then, 0.8 g of 1,1'-carbonyldiimidazole is further added to the mixture and the resultant mixture is refluxed with heating for 20 minutes. The solution is cooled to room temperature. The crystals deposited are separated by filtration, washed with water and dried to obtain 2.50 g of a crude product. The crude product is recrystallized from hot ethanol to obtain 1.75 g of the desired product.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04344948
Source datasetuspto-grants-1982_08
ORD IDord-c835122ef3424078906fed53e8c23d09
Source noteuspto-grants-1982_08