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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 916477Generated: October 29, 2026

Triphenylphosphine → HCID 86597574, compound

https://huagongshe.com/reaction/916477

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriphenylphosphineHCID 11776—
ReactantDiisopropyl diazene-1,2-dicarboxylateHCID 75555—
Reactant3-[4-(2-Fluoroethyl)piperazin-1-YL]propan-1-OLHCID 45115767—
Reactant4-Chloro-6-methoxyquinazolin-7-olHCID 135742251—
SolventDichloromethaneHCID 6344—
ProductHCID 86597574HCID 8659757457%

Reaction Steps

A suspension of 4-chloro-7-hydroxy-6-methoxyquinazoline (202 mg, 0.96 mmol), (prepared as described for the starting material in Example 4), in methylene chloride (10 ml) was treated with triphenylphosphine (352 mg, 1.35 mmol), 3-[4-(2-fluoroethyl)piperazin-1-yl)propan-1-ol (200 mg, 1.06 mmol), (prepared as described for the starting material in Example 27), and diisopropyl azodicarboxylate (226 mg, 1.15 mmol) and the mixture stirred at ambient temperature for 2 hours. The crude reaction mixture was loaded onto a silica column and eluted using methylene chloride/methanol (95/5). The relevant fractions were combined and evaporated under vacuum to give 4-chloro-7-{3-[4-(2-fluoroethyl)piperazin-1-yl]propoxy}-6-methoxyquinazoline (208 mg, 57%) as a white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07268230B2
Source datasetuspto-grants-2007_09
ORD IDord-1a648fd298834a4f8062525c758a2048
Source noteuspto-grants-2007_09