potassium phosphate tribasic monohydrate

O=C(c1ccncc1)c1cc(Cl)ccc1NS(=O)(=O)c1ccc(N2CCCCC2)cc1
Reaction #57808
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2008_09
O=C(c1ccncc1)c1cc(Cl)ccc1NS(=O)(=O)c1ccc(N2CCCC2)cc1
Reaction #57809
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2008_09
O=C(c1ccncc1)c1cc(Cl)ccc1NS(=O)(=O)c1ccc(N2CCS(=O)(=O)CC2)cc1
Reaction #57810
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2008_09
C[C@@H]1CN(c2ccc(S(=O)(=O)Nc3ccc(Cl)cc3C(=O)c3ccncc3)cc2)C[C@H](C)O1
Reaction #57811
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2008_09
O=C(c1ccncc1)c1cc(Cl)ccc1NS(=O)(=O)c1ccc(N2CCSCC2)cc1
Reaction #57812
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2008_09
—
Reaction #57813
amine
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2008_09
O=C(c1ccncc1)c1cc(Cl)ccc1NS(=O)(=O)c1ccc(N2CCC2)cc1
Reaction #57814
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2008_09
C[C@@H]1CN(c2ccc(S(=O)(=O)Nc3ccc(Cl)cc3C(=O)c3cccnc3)cc2)C[C@H](C)O1
Reaction #57816
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2008_09
Cc1ccc(C(=O)c2cc(Cl)ccc2NS(=O)(=O)c2ccc(N3C[C@@H](C)O[C@@H](C)C3)cc2)cn1
Reaction #57817
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2008_09
O=C(c1cccnc1)c1cc(F)c(F)cc1NS(=O)(=O)c1ccc(N2CCOCC2)cc1
Reaction #57819
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2008_09
Cc1ccc(C(=O)c2cc(Cl)ccc2NS(=O)(=O)c2ccc(N3CCOCC3)c(F)c2)cn1
Reaction #57821
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2008_09
Cc1ccc(C(=O)c2cc(Cl)ccc2NS(=O)(=O)c2ccc(N3C[C@@H](C)O[C@@H](C)C3)c(F)c2)cn1
Reaction #57822
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2008_09
C[C@@H]1CN(c2ccc(S(=O)(=O)Nc3ccc(Cl)cc3C(=O)c3cccnc3)cc2F)C[C@H](C)O1
Reaction #57824
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2008_09
COc1ncc(-c2cc(-c3nnc(CN4C[C@@H](C)O[C@@H](C)C4)o3)c3cnn(S(=O)(=O)c4ccc(C)cc4)c3c2)cc1N
Reaction #67135
title compound
Yield 43.6%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_09
COC(=O)c1ccc(C(F)(F)F)cc1C1CC1
Reaction #67702
title compound
Yield 71.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_09
O=S(=O)(Nc1ccc(Cl)cc1-n1nnc2ncccc21)c1ccc(N2CCOCC2)c(F)c1
Reaction #163187
desired product
Yield 44.2%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_09
COc1ccc(-c2cc(-c3ccc(Oc4ccccc4)cc3)c(C#N)c(Cl)n2)cc1
Reaction #168202
2-chloro-6-(4-methoxyphenyl)-4-(4-phenoxyphenyl)nicotinonitrile
Yield 68.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_09
CC(=O)Nc1cccc(-c2cc(-c3ccc(Oc4ccccc4)cc3)c(C#N)c(Cl)n2)c1
Reaction #168206
N-(3-(6-chloro-5-cyano-4-(4-phenoxyphenyl)pyridin-2-yl)phenyl)acetamide
Yield 42.7%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_09
O=S(=O)(Nc1ccc(Cl)cc1-n1nnc2ncccc21)c1ccc(N2CCOCC2)c(F)c1
Reaction #305388
desired product
Yield 44.2%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2012_06
CC(=O)c1ccccc1-c1ccc(C#N)cc1
Reaction #357803
2′-acetyl-4-biphenylcarbonitrile
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2008_11
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