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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 406759Generated: October 30, 2026

2,2'-Bipyridine → 1-cyclopropyl-4-iodopyridin-2(1H)-one

https://huagongshe.com/reaction/406759

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2,2'-BipyridineHCID 1474—
ReactantSodium CarbonateHCID 10340—
ReactantCyclopropylboronic acidHCID 2760897—
Reactant4-Iodo-1,2-dihydropyridin-2-oneHCID 20582535—
CatalystCupric acetateHCID 8895—
Solvent1,1-DichloroethaneHCID 6365—
Product1-cyclopropyl-4-iodopyridin-2(1H)-oneHCID 5919037681%

Reaction Conditions

Temperature70 °C

Reaction Steps

A mixture of 4-iodopyridin-2(1H)-one (0.2425 g, 1.10 mmol, 1.0 equiv), Cu(OAc)2 (0.2146 g, 1.18 mmol, 1.07 equiv), bipyridine (0.1832 g, 1.17 mmol, 1.07 equiv), cyclopropylboronic acid (0.2122 g, 2.47 mmol, 2.25 equiv) and Na2CO3 (0.2638 g, 2.49 mmol, 2.27 equiv) in dichloroethane (10 mL) was stirred at 70° C. for 18 h. The reaction mixture was quenched with satd aq NH4Cl, diluted with CH2Cl2, and dried over Na2SO4. After the solvent was removed under reduced pressure, the residue was purified by chromatography on silica gel eluted with hexanes/ethyl acetate to afford 0.2309 g (81%) of 1-cyclopropyl-4-iodopyridin-2(1H)-one. Step 2

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08754076B2
Source datasetuspto-grants-2014_06
ORD IDord-71d90882133443c3a4a4ee28803786c2
Source noteuspto-grants-2014_06