反应 #43338

ord-346479f217a54dc0be427131770c50f8

反应方程式

O=c1cc(OCc2ccccc2)ccn1-c1ccc(O)cc1
4-benzyloxy-1-(4-hydroxyphenyl)-1H-pyridin-2-one
CCN(CC)CCO
2-(diethylamino)ethanol
Fc1ccc(OCc2ccnc(Cl)c2)cc1
( 2 )
Fc1ccc(OCc2ccnc(Cl)c2)cc1
2-chloro-4-[(4-fluorophenoxy)methyl]pyridine
Fc1ccc(CBr)cc1
4-fluorobenzyl bromide
CS(=O)(=O)OCc1ccccn1
2-methanesulfonyloxymethylpyridine
CCN(CC)CCOc1ccc(-n2ccc(OCc3ccccn3)cc2=O)cc1
title compound
CCN(CC)CCOc1ccc(-n2ccc(OCc3ccccn3)cc2=O)cc1
4-(2-Pyridinylmethoxy)-1-{4-[2-(diethylamino)ethoxy]phenyl}-1H-pyridin-2-one

反应条件

详细条件
See reaction.notes.procedure_details.

实验过程

Steps (1) and (2) of Example 28 were repeated except that 4-fluorobenzyl bromide used in Example 28 was replaced with 2-methanesulfonyloxymethylpyridine, and successively Example 12 was repeated except that so obtained compound was used in place of 4-benzyloxy-1-(4-hydroxyphenyl)-1H-pyridin-2-one in Step (3) and 2-(1-pyrrolidine)ethanol was replaced with 2-(diethylamino)ethanol, to provide the title compound.

来源

DOI: 10.6084/m9.figshare.5104873.v1专利: US07732456B2uspto-grants-2010_06