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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2182562Generated: November 2, 2026

Dichloromethane → Quinazoline hydrochloride

https://huagongshe.com/reaction/2182562

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDichloromethaneHCID 6344—
ReactantTriphenylphosphineHCID 11776—
Reactantethyl N-ethoxycarbonyliminocarbamateHCID 220568—
Reactant1-(3-Hydroxypropyl)pyrrolidin-2-oneHCID 566744—
Reactant4-(4-Bromo-2-fluoroanilino)7-hydroxy-6-methoxyquinolineHCID 136411682—
ProductQuinazoline hydrochlorideHCID 2118698367%

Reaction Steps

Using a method analogous to that in Example 47, 4-(4-bromo-2-fluoroanilino)7-hydroxy-6-methoxyquinoline (146 mg, 0. mmol) in methylene chloride (5 ml) was treated with 1-(3hydroxypropyl)-2-pyrrolidinone (86 mg, 0.6 mmol), triphenylphosphine (314 mg, 1.2 mmol) and diethyl azodicarboxylate (209 mg, 1.2 mmol) and was purified and isolated to give 4-(4-bromo-2-fluoroanilino)-methoxy-73(oxopyrrolidin-1-yl)propoxy)quinazoline hydrochloride (140 mg, 67%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06897210B2
Source datasetuspto-grants-2005_05
ORD IDord-33fcd66a73d04b5bb83ca849b9eeb3f2
Source noteuspto-grants-2005_05