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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 505329Generated: November 2, 2026

Dichloromethane → HCID 178433171, compound

https://huagongshe.com/reaction/505329

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDichloromethaneHCID 6344—
ReactantSodium HydroxideHCID 14798—
Reactant2-PhenoxyethanamineHCID 15651—
ReactantHCID 178503328HCID 178503328—
CatalystHydrogen PeroxideHCID 784—
SolventAcetonitrileHCID 6342—
ProductHCID 178433171HCID 17843317147%

Reaction Conditions

Temperature200 °C

Reaction Steps

8-Bromo-6-chloro-4-methyl-2-methylsulfanyl-3,4-dihydro-quinazoline hydroiodide (141 mg, 0.33 mmol) and 2-phenoxyethyl amine (53.5 mg, 0.39 mmol) were dissolved in acetonitrile (1 ml) and heated to 200° C. in a sealed tube in a microwave oven for 30 minutes. After cooling the reaction was treated with 1N aqueous sodium hydroxide solution, methylene chloride and 5 to 7 drops of 30% aqueous hydrogen peroxide solution. After the reaction has ceased the layers were separated and the aqueous phase was extracted with methylene chloride. The combined organic layers were dried over sodium sulfate, filtered, the solvent was evaporated and the residue was purified by column chromatography (CH2Cl2:MeOH:aq conc NH3=9:1:0.1) to yield the title compound as an off-white solid (60 mg, 47%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07781441B2
Source datasetuspto-grants-2010_08
ORD IDord-c91c674f21094a928dd3ad36b2a9e099
Source noteuspto-grants-2010_08