Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1838592Generated: October 31, 2026

Triphenylphosphine → HCID 5329030, compound

https://huagongshe.com/reaction/1838592

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriphenylphosphineHCID 11776—
Reactant4-Piperidinol, 1-methyl-HCID 66048—
Reactantethyl N-ethoxycarbonyliminocarbamateHCID 220568—
Reactant4-(4-Chloro-2-fluorophenylamino)-7-hydroxy-6-methoxyquinazolineHCID 135513720—
SolventDichloromethaneHCID 6344—
ProductHCID 5329030HCID 532903086.4%

Reaction Conditions

Temperature5 °C

Reaction Steps

Diethyl azodicarboxylate (218 mg, 1.25 mmol) was added dropwise to a solution of 4-(4-chloro-2-fluoroanilino)-7-hydroxy-6-methoxyquinazoline (159 mg, 0.5 mmol), (prepared as described for the starting material in Example 2), 4-hydroxy-1-methylpiperidine (115 mg, 1 mmol) and triphenylphosphine (328 mg, 1.25 mmol) in methylene chloride (5 ml) cooled at 5° C. under nitrogen. The mixture was stirred for 1 hour at ambient temperature, the solvent was removed by evaporation and the residue was partitioned between 2M hydrochloric acid and ether. The aqueous layer was separated, adjusted to pH9 with aqueous sodium hydrogen carbonate solution and extracted with methylene chloride. The methylene chloride layer was washed with brine, dried (MgSO4) and the solvent removed by evaporation. The residue was purified on neutral alumina eluting with- methylene chloride/methanol (97/3). The purified product was triturated with ether, collected by filtration and dried to give 4-(4chloro-2-fluoroanilino)-6-methoxy-7-(1-methylpiperidin-4-yloxy)quinazoline (180 mg, 79%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06673803B2
Source datasetuspto-grants-2004_01
ORD IDord-12fe14cde6494ed89d8f05e878f215fd
Source noteuspto-grants-2004_01