Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1798516Generated: October 25, 2026

Sodium Carbonate → HCID 68737237, compound

https://huagongshe.com/reaction/1798516

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium CarbonateHCID 10340—
Reactant(5''-Bromo-[2,2';4',3'']terpyridin-6'-yl)-cyclopropyl-amineHCID 44135953—
ReactantDimethyl((2-(3-(tetramethyl-1,3,2-dioxaborolan-2-yl)phenoxy)ethyl))amineHCID 54594420—
Solvent1,2-DimethoxyethaneHCID 8071—
SolventEthyl AcetateHCID 8857—
ProductHCID 68737237HCID 68737237—

Reaction Steps

To a solution of Dimethyl-(2-[3-(4,4,5,5-tetramethyl-[1,3,2]dioxaborolan-2-yl)-phenoxy]-ethyl)-amine (2 eq, 0.272 mmol, 0.079 g) in dry DME (1 ml) under an inert atmosphere of argon is added 2M Na2CO3 (3 eq, 0.408 mmol, 0.204 ml) followed by (5″-Bromo-[2,2′;4′,3″]terpyridin-6′-yl)-cyclopropyl-amine (Example 1.26) (1 eq, 0.136 mmol, 50 mg) and PdCl2dppf (0.1 eq, 0.014 mmol, 11 mg). The reaction mixture is heated using microwave radiation at 90° C. for 90 minutes. The reaction mixture is dissolved in EtOAc and washed with water. The organic solvent is reduced in vacuo and the residue is purified by reverse phase column chromatography (Isolute™ C18, 0-40% 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]+ 452.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08343966B2
Source datasetuspto-grants-2013_01
ORD IDord-5139c39e225745b1aafd71465d6f58f7
Source noteuspto-grants-2013_01