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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2182575Generated: October 29, 2026

Dichloromethane → HCID 178496235, compound

https://huagongshe.com/reaction/2182575

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDichloromethaneHCID 6344—
ReactantDiethylene Glycol Monomethyl EtherHCID 8134—
ReactantTriphenylphosphineHCID 11776—
Reactantethyl N-ethoxycarbonyliminocarbamateHCID 220568—
Reactant4-[(4-Bromo-2-fluorophenyl)amino]-6-methoxy-7-quinazolinolHCID 135503852—
ProductHCID 178496235HCID 17849623534%

Reaction Steps

Diethyl azodicarboxylate (236 μl, 1.5 mmol) was added dropwise to a mixture of 4-(4-bromo-2-fluoroanilino)-7-hydroxy-6-methoxyquinazoline (182 mg, 0.5 mmol), (prepared as described for the starting material in Example 48), triphenylphosphine (393 mg, 1.5 mmol) and 2-(2-methoxyethoxy)ethanol (84 μl, 0.7 mmol) in methylene chloride (7 ml) under nitrogen. The mixture was stirred for 4 hours at ambient temperature, the reaction mixture was purified by pouring it directly on to a column of silica and eluting with ethyl acetate/petroleum ether (9/1 followed by 10/0). The purified product was tri ed with ether and collected by filtration. The solid was dissolved in methylene chloride/methanol and 2M ethereal hydrogen chloride (1 ml) was added. The mixture was concentrated by evaporation and the precipitate was collected by filtration, washed with ether and dried under vacuum to give 4-(4-bromo-2-fluoroanilino)4-methoxy-7-(2-(2-methoxyethoxy)ethoxy)quinazoline hydrochloride (84 mg, 34%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06897210B2
Source datasetuspto-grants-2005_05
ORD IDord-669aafb7d0154d9fb2ba503ca19e01cd
Source noteuspto-grants-2005_05