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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2182556Generated: November 2, 2026

Dimethylformamide → HCID 22478210, compound

https://huagongshe.com/reaction/2182556

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethylformamideHCID 6228—
ReactantMorpholineHCID 8083—
Reactant1,3-Propanediamine, N'-(ethylcarbonimidoyl)-N,N-dimethyl-, monohydrochlorideHCID 2723939—
Reactant7-(3-Carboxypropoxy)-4-(4-chloro-2-fluoroanilino)-6-methoxyquinazolineHCID 22478293—
Catalyst4-(Dimethylamino)pyridineHCID 14284—
ProductHCID 22478210HCID 2247821046%

Reaction Steps

1-(3-Dimethylaminopropyl)3-ethylcarbodiimide hydrochloride (94 mg, 4.9 mmol) was added to a mixture of 7-(3-carboxypropoxy)-4-(4-chloro-2-fluoroanilino)-6-methoxyquinazoline (164 mg, 0.4 mmol), morpholine (0.11 g; 1.26 mmol) and 4-dimethylaminopyridine (200 mg, 1.64 mmol) in DMF (5 ml). The reaction mixture was stirred at ambient temperature for 24 hours and the volatiles were removed by evaporation. Water was added to the residue and the aqueous mixture was extracted with methylene chloride (3×30 ml). The extracts were combined and the solvent removed by evaporation. The residue was triturated with ether and the precipitate was collected by filtration. The solid was purified by column chromatography eluting with methylene chloride/methanol/aqueous ammonia (100/8/1). The purified product was triturated with acetone, collected by filtration and dried to give 4-(4-chloro-2-fluoroanilino)-methoxy-7-(3-morpholinocarbonylpropoxy)quinazoline (88 mg, 46%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06897210B2
Source datasetuspto-grants-2005_05
ORD IDord-5ec7208b4e7e4042ac83e534282b825c
Source noteuspto-grants-2005_05