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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1414237Generated: November 1, 2026

Sodium Hydroxide → 2-(1-Piperazinyl)-4-amino-6,7-dimethoxyquinazoline

https://huagongshe.com/reaction/1414237

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium HydroxideHCID 14798—
Reactant2-Chloro-6,7-dimethoxy-4-quinazolinamineHCID 90235—
ReactantPiperazine--hydrogen bromide (1/1)HCID 3014804—
SolventWaterHCID 962—
Solvent2-MethoxyethanolHCID 8019—
Product2-(1-Piperazinyl)-4-amino-6,7-dimethoxyquinazolineHCID 616267—

Reaction Conditions

Temperature75 °C

Reaction Steps

Piperazine hydrobromide (168.0 g., 1.006 mole) was added to a suspension of 4-amino-2-chloro-6,7-dimethoxyquinazoline (241.0 g., 1.006 mole) in 2-methoxyethanol (3.6 l.) and the mixture was stirred at reflux for 1.25 hours. The precipitate was separated by filtration, washed with hot 2-methoxyethanol and dried. The material then was added to a stirred solution of sodium hydroxide (81.0 g., 2.01 mole) in water (3 l.) and the mixture was heated to 75° C. The mixture then was cooled to 40° C., filtered, and the insoluble precipitate washed with water and dried. The material was triturated under refluxing absolute ethanol (6.0 l.) and the mixture was filtered. The filtrate was evaporated to dryness to yield the title compound, 180.0 g. (62%), M.P. 224°-228° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04001238
Source datasetuspto-grants-1977_01
ORD IDord-c8156cdc59b7426ba17db8c58dbc4bca
Source noteuspto-grants-1977_01