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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1351210Generated: November 2, 2026

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

https://huagongshe.com/reaction/1351210

Reaction equation

Participants

RoleNameHCIDCharge
ReactantO-XyleneHCID 7237—
Reactant(6-Allyloxy-7-methoxy-quinazolin-4-yl)-(3-chloro-4-fluoro-phenyl)-amineHCID 21098401—
Product5-Allyl-4-(3-chloro-4-fluoro-phenylamino)-7-methoxy-quinazolin-6-olHCID 11462529—

Reaction Steps

A solution of (6-allyloxy-7-methoxy-quinazolin-4-yl)-(3-chloro-4-fluoro-phenyl)-amine (0.92 g, 2.55 mmol) (from Example 18, Step C, supra) in o-xylene (150 mL) was heated at 150° C. for 7 hours. At the end of this period, 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-chloro-4-fluoro-phenylamino)-7-methoxy-quinazolin-6-ol as an off white solid. (Yield 0.65 g, 71%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07217717B2
Source datasetuspto-grants-2007_05
ORD IDord-09ea2d8b417a48c78b48bc0f6ef45f3b
Source noteuspto-grants-2007_05