Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1351192Generated: November 2, 2026

Methyl iodide → HCID 11174663, compound

https://huagongshe.com/reaction/1351192

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl iodideHCID 6328—
ReactantPotassium CarbonateHCID 11430—
ReactantHCID 21098393HCID 21098393—
SolventAcetoneHCID 180—
ProductHCID 11174663HCID 11174663—

Reaction Conditions

Temperature90 °C

Reaction Steps

To a solution of 5-allyl-7-methoxy-4-phenylamino-quinazolin-6-ol (0.16 g, 0.524 mmol) (from Example 15, Step D, supra) in acetone (30 mL) was added K2CO3 (0.36 g, 2.62 mmol) and methyl iodide (0.15 g, 1.05 mmol) (Aldrich). The reaction mixture was heated with stirring at 90° C. for 4 hours. The mixture was cooled to room temperature, filtered and the filtrate was concentrated. The residue was purified by chromatography using EtOAc/CH2Cl2/Et3N (1:5:0.05) as eluent to give the desired (5-allyl-6,7-dimethoxy-quinazolin-4-yl)-phenyl-amine as a pale yellow solid. (Yield 0.13 g, 77%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07217717B2
Source datasetuspto-grants-2007_05
ORD IDord-dae9a2ec8d2e499bbf204467a9e322e0
Source noteuspto-grants-2007_05