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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 363753Generated: October 26, 2026

Quinazoline → 2,4-Diamino-5-chloro-6-(5-chloro-2-hydroxyphenyl)quinazoline

https://huagongshe.com/reaction/363753

Reaction equation

Participants

RoleNameHCIDCharge
ReactantQuinazolineHCID 9210—
ReactantBoron tribromideHCID 25134—
Reactant2,4-Diamino-5-chloro-6-(5-chloro-2-methoxyphenyl)quinazolineHCID 54072668—
SolventDichloromethaneHCID 6344—
Product2,4-Diamino-5-chloro-6-(5-chloro-2-hydroxyphenyl)quinazolineHCID 54369095—

Reaction Steps

A series of quinazoline analogs may be prepared from the above 2,4-diamino-5-chloro-6-(5-chloro-2-methoxyphenyl)quinazoline. This is accomplished by the reaction of 2,4-diamino-5-chloro-6-(5-chloro-2-methoxyphenyl)quinazoline with 1M boron tribromide in methylene chloride, yielding the corresponding 2,4-diamino-5-chloro-6-(5-chloro-2-hydroxyphenyl)quinazoline. The hydroxy intermediate in turn is reacted with a halogen-containing compound and potassium carbonate in N,N-dimethylformamide, affording the appropriately 6-(5-chloro-2-substituted-phenyl)quinazoline, for example, 2,4-diamino-5-chloro-6-[5-chloro-2-(pyridin-2-ylmethoxy)phenyl]quinazoline. Example 3 describes in detail the preparation of this compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05874579
Source datasetuspto-grants-1999_02
ORD IDord-82fbf7dfff9349dfb0fd2389869a69ca
Source noteuspto-grants-1999_02