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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2182551Generated: November 3, 2026

Dichloromethane → HCID 86759736, compound

https://huagongshe.com/reaction/2182551

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDichloromethaneHCID 6344—
ReactantTributylphosphineHCID 13831—
Reactantdiazenedicarboxylic acid bis(N,N-piperidide)HCID 5702657—
Reactant2-(Cyclopentyloxy)ethan-1-olHCID 13187520—
ReactantHCID 136399837HCID 136399837—
SolventDiethyl EtherHCID 3283—
ProductHCID 86759736HCID 8675973660%

Reaction Steps

1,1-(Azodicarbonyl)dipiperidine (355 mg, 1.4 mmol) was added in portions to a mixture of 44-chloro-2-fluoroanilino)-7-hydroxy-methoxyquinazoline (I 50 mg, 0.47 mmol), (prepared as described for the starting material in Example 2), 2-(cyclopentyloxy)ethanol (91 mg, 0.7 mmol), (U.S. Pat. No. 4,515,814), and tributylphosphine (284 mg, 1.4 mmol) in methylene chloride (6 ml) at 0° C. The mixture was then allowed to warm to ambient temperature and stirred for 3.5 hours. Ether (3 ml) was added and the insolubles were removed by filtration and the volatiles were removed from the filtrate by evaporation. The residue was dissolved in acetone and 1M ethereal hydrogen chloride (0.6 ml) was added. The mixture was left to stand for 60 hours and the precipitate was collected by filtration, washed with acetone and dried to give 44-chloro-2-fluoroanilino)-72-cyclopentyl xyethoxy)-4-methoxyquinazoline hydrochloride (130 mg, 60%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06897210B2
Source datasetuspto-grants-2005_05
ORD IDord-f468ebb7b5a242c2ae43886d535a358b
Source noteuspto-grants-2005_05