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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 921007Generated: November 2, 2026

2,2'-Bipyridine → HCID 71063089, compound

https://huagongshe.com/reaction/921007

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2,2'-BipyridineHCID 1474—
ReactantSodium CarbonateHCID 10340—
ReactantCyclopropylboronic acidHCID 2760897—
Reactant5-bromo-1H-pyrrolo[2,3-b]pyridineHCID 10307932—
CatalystCupric acetateHCID 8895—
Solvent1,1-DichloroethaneHCID 6365—
ProductHCID 71063089HCID 7106308931.5%

Reaction Conditions

Temperature110 °C

Reaction Steps

Cyclopropylboronic acid (0.872 g, 10.15 mmol) was added to a solution of 5-bromo-1H-pyrrolo[2,3-b]pyridine (1 g, 5.08 mmol), Na2CO3 (1.076 g, 10.15 mmol), copper(II)acetate (0.922 g, 5.08 mmol) and 2,2′-bipyridine (0.793 g, 5.08 mmol) in dichloroethane (20 mL), and the mixture was stirred at 110° C. for 8 h. The reaction mixture was concentrated, and then diluted with ethyl acetate and water. Organic layer was separated, washed with brine, dried over Na2SO4 and filtered. The filtrate was concentrated in reduced pressure and purified by flash chromatography using 10% ethyl acetate in pet ether to afford title compound (0.38 g, 31.3%) as oil. 1H NMR (300 MHz, CDCl3): δ 8.38 (d, J=2.1 Hz, 1H), 7.99 (d, J=2.1 Hz, 1H), 7.20 (d, J=3.3 Hz, 1H), 6.34 (d, J=3.6 Hz, 1H), 3.5 (m, 1H), 1.15 (m, 2H), 1.03 (m, 2H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09273069B2
Source datasetuspto-grants-2016_03
ORD IDord-4b7a9f999dd743968b40519c08de3d69
Source noteuspto-grants-2016_03