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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1072418Generated: November 4, 2026

4-Pyridinemethanamine → [7-(3,4-Dimethoxy-phenyl)-imidazo[1,2-c]pyrimidin-5-yl]pyridin-4-ylmethyl-amine

https://huagongshe.com/reaction/1072418

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-PyridinemethanamineHCID 77317—
ReactantDiisopropylethylamineHCID 81531—
Reactant5-Chloro-7-(3,4-dimethoxyphenyl)imidazo[1,2-c]pyrimidineHCID 22386546—
SolventIsopropanolHCID 3776—
Product[7-(3,4-Dimethoxy-phenyl)-imidazo[1,2-c]pyrimidin-5-yl]pyridin-4-ylmethyl-amineHCID 1793186652.6%

Reaction Conditions

Temperature90 °C

Reaction Steps

The mixture of 5-chloro-7-(3,4-dimethoxyphenyl)-imidazo[1,2-c]pyrimidine (57.94 mg, 0.2 mmol), 4-aminomethylpyridine (23.79 mg, 0.22 mmol), and diisopropylethylamine (38.78, 0.3 mmol) in 2-propanol was stirred at 90° C. for 20 h, and cooled to room temperature. The solvent was evaporated, and 5 ml of ice water was added. Then the resulting product was extracted with 2×10 ml of ethyl acetate. The combined extract was dried over MgSO4. Then the solvent was evaporated and 2 ml of ether was added. The produced solid was collected by filtration and dried to give pure product (38 mg, 52.6%) of [7-(3,4-dimethoxy-phenyl)-imidazo[1,2-c]pyrimidin-5-yl]pyridin-4-ylmethyl-amine.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06911443B2
Source datasetuspto-grants-2005_06
ORD IDord-5ace11e4df714cb885be6f4f3d0af7a1
Source noteuspto-grants-2005_06