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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1166151Generated: October 30, 2026

1-Benzylpiperazine → 2-(4-Chlorophenyl)-4-(4-benzylpiperazino)-6,7,8-trimethoxyquinazoline

https://huagongshe.com/reaction/1166151

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-BenzylpiperazineHCID 75994—
Reactant2-(4-Chlorophenyl)-4-chloro-6,7,8-trimethoxyquinazolineHCID 11783471—
Product2-(4-Chlorophenyl)-4-(4-benzylpiperazino)-6,7,8-trimethoxyquinazolineHCID 11123999—

Reaction Conditions

Temperature150 °C

Reaction Steps

A mixture of 2.0 g of 2-(4-chlorophenyl)-4-chloro-6,7,8-trimethoxyquinazoline and 5.0 g of N-benzylpiperazine was heated at 150° C. for 1 h. After cooling, 20 ml of ice water were added and the mixture was extracted with ethyl acetate. The organic phase was dried over sodium sulfate and concentrated. The oily crude product thus obtained was recrystallized from isopropanol. Yield: 1 g. M.p.: 150° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06613772B1
Source datasetuspto-grants-2003_09
ORD IDord-6747592a7e76453cb68696400a8b36fa
Source noteuspto-grants-2003_09