6-phenoxy-3-pyridine sulfonyl chloride

CCc1cc(O)c(F)cc1-c1ccc2c(-c3nc4c([nH]3)CCN(S(=O)(=O)c3ccc(Oc5ccccc5)nc3)C4)n[nH]c2c1
Reaction #427196
title compound
收率 17.2%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_11
CCc1cc(O)c(F)cc1-c1ccc2c(-c3nc4c([nH]3)CCN(S(=O)(=O)c3ccc(Oc5ccccc5)nc3)C4)n[nH]c2c1
Reaction #886323
DOI: 10.1039/C8SC04228DTest data from https://doi.org/10.1039/C8SC04228D
CN(C)CC(CC(=O)OCc1ccccc1)NS(=O)(=O)c1ccc(Oc2ccccc2)nc1
Reaction #888251
DOI: 10.1039/C8SC04228DTest data from https://doi.org/10.1039/C8SC04228D
NC(=O)c1ccccc1
Reaction #1018647
benzamide
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2016_03
CC1(C)[C@@H]2C[C@H]3OB([C@H](CC4CCC4)NC(=O)[C@H](Cc4ccccc4)NS(=O)(=O)c4ccc(Oc5ccccc5)nc4)O[C@@]3(C)[C@H]1C2
Reaction #1269877
desired product
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_03
CN(C)C[C@@H](CC(=O)OCc1ccccc1)NS(=O)(=O)c1ccc(Oc2ccccc2)nc1
Reaction #2045899
title compound
收率 37.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_04
CCc1cc(O)c(F)cc1-c1ccc2c(-c3nc4c([nH]3)CCN(S(=O)(=O)c3ccc(Oc5ccccc5)nc3)C4)n[nH]c2c1
Reaction #2125845
title compound
收率 17.2%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_11