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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1351205Generated: November 3, 2026

O-Xylene → 5-Allyl-4-(3-bromo-phenylamino)-7-methoxy-quinazolin-6-ol

https://huagongshe.com/reaction/1351205

Reaction equation

Participants

RoleNameHCIDCharge
ReactantO-XyleneHCID 7237—
Reactant(6-Allyloxy-7-methoxy-quinazolin-4-yl)-(3-bromo-phenyl)-amineHCID 21098400—
Product5-Allyl-4-(3-bromo-phenylamino)-7-methoxy-quinazolin-6-olHCID 11269168—

Reaction Steps

A solution of (6-allyloxy-7-methoxy-quinazolin-4-yl)-(3-bromo-phenyl)-amine (0.54 g, 1.39 mmol) (from Example 17, Step C, supra) in o-xylene (75 mL) was heated at 150° C. for 4.5 hours, during which time TLC analysis indicated almost complete consumption of the starting material and the formation of desired product as the major spot. The solution was concentrated and filtered. The solid was collected and dried in vacuo to give the desired 5-allyl-4-(3-bromo-phenylamino)-7-methoxy-quinazolin-6-ol as an off white solid. (Yield 0.33 g, 61%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07217717B2
Source datasetuspto-grants-2007_05
ORD IDord-804443d7e37d4a0da1d83f566fa2395e
Source noteuspto-grants-2007_05