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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1175073Generated: November 3, 2026

HCID 67415371, compound → HCID 136383504, compound

https://huagongshe.com/reaction/1175073

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 67415371HCID 67415371—
SolventTrifluoroacetic acidHCID 6422—
ProductHCID 136383504HCID 136383504—

Reaction Steps

A solution of 7-(benzyloxy)-N-(3-chloro-2-fluorophenyl)-6-methoxyquinazolin-4-amine hydrochloride 2 (85.45 g, 0.192 mol) in trifluoroacetic acid (300 mL) was heated at 80° C. for 1 hour. The reaction mixture was the evaporated to dryness and the residues re-dissolved in methanol (200 mL). This solution was then added dropwise to a stirred aqueous solution of saturated sodium bicarbonate (500 mL). The resulting precipitate was collected by filtration, washed with acetonitrile and dried under vacuum. The crude solids were then purified by hot (100° C.) trituration with a mixture of butanone (500 mL) and MeOH (100 mL), filtered and dried to 4-[(3-chloro-2-fluorophenyl)amino]-6-methoxyquinazolin-7-ol 3 as a cream solid (45 g, 73%); 1H NMR Spectrum: (DMSO d6): 3.98 (s, 3H), 7.10 (s, 1H), 7.25-7.30 (m, 1H), 7.40-7.50 (m, 1H), 7.50-7.60 (m, 1H), 7.80 (s, 1H), 8.30 (s, 1H), 9.55 (s, 1H), 10.32 (s, 1H); Mass Spectrum: (M+H)+ 319.98

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07838530B2
Source datasetuspto-grants-2010_11
ORD IDord-16271a6275f14d8f985851010f38f3f4
Source noteuspto-grants-2010_11