Welcome to chemicalbook!
Chinese English Japanese Germany Korea
400-158-6606
Try our best to find the right business for you.
Do not miss inquiry messages Please log in to view all inquiry messages.

Welcome back!

1-Cyclopropyl-4-iodopyridin-2(1H)-one synthesis

2synthesis methods
858839-90-4 Synthesis
4-IODO-2-PYRIDONE

858839-90-4
89 suppliers
$52.00/250mg

411235-57-9 Synthesis
Cyclopropylboronic acid

411235-57-9
426 suppliers
$6.00/1g

1-Cyclopropyl-4-iodopyridin-2(1H)-one

1193335-00-0
2 suppliers
inquiry

-

Yield:1193335-00-0 81%

Reaction Conditions:

with copper diacetate;sodium carbonate in 1,2-dichloro-ethane at 70; for 18 h;

Steps:

85.1

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.

References:

US2010/331320,2010,A1 Location in patent:Page/Page column 96

858839-90-4 Synthesis
4-IODO-2-PYRIDONE

858839-90-4
89 suppliers
$52.00/250mg

411235-57-9 Synthesis
Cyclopropylboronic acid

411235-57-9
426 suppliers
$6.00/1g

1-Cyclopropyl-4-iodopyridin-2(1H)-one

1193335-00-0
2 suppliers
inquiry