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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1798513Generated: October 29, 2026

Potassium Carbonate → Cyclopropyl-(5''-ethynyl-[2,2';4',3'']terpyridin-6'-yl)-amine

https://huagongshe.com/reaction/1798513

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
ReactantCyclopropyl-(5''-trimethylsilanylethynyl-[2,2';4',3'']terpyridin-6'-yl)-amineHCID 68947114—
SolventMethanolHCID 887—
SolventEthyl AcetateHCID 8857—
ProductCyclopropyl-(5''-ethynyl-[2,2';4',3'']terpyridin-6'-yl)-amineHCID 86633651—

Reaction Steps

Cyclopropyl-(5″-trimethylsilanylethynyl-[2,2′;4′,3″]terpyridin-6′-yl)-amine (Example 2.128, step1) (1 eq, 0.127 mmol, 49 mg) is dissolved in MeOH (2 ml) and potassium carbonate is added (2 eq, 0.255 mmol, 35 mg). The reaction mixture is dissolved in EtOAc and washed with water. The organic layer is washed with brine, dried over drying agent MgSO4, filtered and the organic solvent is reduced in vacuo. The crude residue is purified by reverse phase column chromatography (Isolute™ C18, 0-20% acetonitrile in water—0.1% TFA). The appropriate fractions by HPLC are combined and concentrated in vacuo. The resulting residue is dissolved in MeOH and loaded onto a SCX-2 cartridge eluting with MeOH followed by 2M NH3 in MeOH. The methanolic ammonia fractions are combined, concentrated in vacuo and dried under vacuum to afford the title compound; [M+H]+ 313.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08343966B2
Source datasetuspto-grants-2013_01
ORD IDord-7cb0218a28bb47e693f9f4cb5729e5ee
Source noteuspto-grants-2013_01