Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1288870Generated: November 3, 2026

4-Chloro-6,7-dimethoxyquinazoline → (6,7-Dimethoxyquinazolin-4-yl)-(3-ethynylphenyl)-amine Hydrochloride

https://huagongshe.com/reaction/1288870

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-Chloro-6,7-dimethoxyquinazolineHCID 2769364—
Reactant4-Fluoro-3-((trimethylsilyl)ethynyl)anilineHCID 12687358—
Solventtert-ButanolHCID 6386—
Product(6,7-Dimethoxyquinazolin-4-yl)-(3-ethynylphenyl)-amine HydrochlorideHCID 18925020—

Reaction Steps

4-Chloro-6,7-dimethoxyquinazoline (500 mg, 2.23 mmol) and 3-(2'-trimethylsilylethynyl)-4-fluoroaniline (507 mg, 2.44 mmol) were refluxed in 5 mL of tert-butyl alcohol for 16 hours, cooled and filtered to afford solid (6,7-dimethoxy-quinazolin-4-yl)-(3'-ethynyl-phenyl)-amine hydrochloride which was washed with 10 mL of isopropyl alcohol and dried in vacuo at 70° C., 832 mg (83%). This was reacted in 10 mL of methanol and 1 drop of water containing 250 mg of potassium carbonate for 3 hours. The mixture was filtered and the filtrate vacuum evaoprated. This residue was triturated for 1 hour with 1N hydrochloric acid, filtered and washed with a minimum amount of water then methanol and dried in vacuo; 506 mg (63%) mp 229° C. dec.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05747498
Source datasetuspto-grants-1998_05
ORD IDord-b45d0822636c4ed0ac97cc0bb88de1a0
Source noteuspto-grants-1998_05