Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 470548Generated: October 29, 2026

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

https://huagongshe.com/reaction/470548

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 numberUS08629138B2
Source datasetuspto-grants-2014_01
ORD IDord-0782ef9a29664f81b80e9d290a6e2e49
Source noteuspto-grants-2014_01