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
Participants
| Role | Name | HCID | Charge |
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| Reactant | 2,2'-Bipyridine | HCID 1474 | — |
| Reactant | Sodium Carbonate | HCID 10340 | — |
| Reactant | Cyclopropylboronic acid | HCID 2760897 | — |
| Reactant | 4-Iodo-1,2-dihydropyridin-2-one | HCID 20582535 | — |
| Catalyst | Cupric acetate | HCID 8895 | — |
| Solvent | 1,1-Dichloroethane | HCID 6365 | — |
| Product | 1-cyclopropyl-4-iodopyridin-2(1H)-one | HCID 59190376 | 81% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08629138B2 |
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| Source dataset | uspto-grants-2014_01 |
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| ORD ID | ord-0782ef9a29664f81b80e9d290a6e2e49 |
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| Source note | uspto-grants-2014_01 |
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