EtOH AcOH

CC(=O)NC(Cc1ccc(O)cc1)C(=O)NC(Cc1ccc(F)cc1)C(=O)N1CC(Cc2ccc3ccccc3c2)NC(=O)C1Cc1c[nH]cn1
Reaction #8632
desired product
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
CCCOc1ccc(-c2ccc(-c3ccccc3Cl)n2Cc2ccc(OCCO)c(N)n2)cc1
Reaction #43293
solid
Ausbeute 39.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
Cc1ccc(S(=O)(=O)OCC2COc3ccc4ncccc4c3O2)cc1
Reaction #56739
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2008_09
Cc1ccc(S(=O)(=O)OCC2COc3ccc4nc(C)ccc4c3O2)cc1
Reaction #56741
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2008_09
CCN(c1ccccc1)S(=O)(=O)c1ccc(-n2[nH]c(C)c(C(C)(C)c3ccccc3)c2=O)nc1
Reaction #73498
N-ethyl-6-[3-methyl-4-(1-methyl-1-phenylethyl)-5-oxo-2,5-dihydro-1H-pyrazol-1-yl]-N-phenylpyridine-3-sulfonamide
Ausbeute 44.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_09
Cc1[nH]n(-c2ccc(S(=O)(=O)N(C)C)cn2)c(=O)c1Cc1cccnc1
Reaction #73502
N,N-dimethyl-6-[3-methyl-5-oxo-4-(pyridin-3-ylmethyl)-2,5-dihydro-1H-pyrazol-1-yl]pyridine-3-sulfonamide
Ausbeute 28.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_09
CC(=O)c1c(O)c2ccccc2n1-c1ccccc1
Reaction #75008
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1979_11
—
Reaction #90867
DA168
Ausbeute 73.5%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2016_09
Nc1cc(F)ccc1Br
Reaction #219419
expected product
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2008_06
COC(=O)c1cccc(Cl)c1N
Reaction #219428
expected product
Ausbeute 79.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2008_06
COC(=O)c1c(N)cccc1F
Reaction #219433
methyl 2-amino-6-fluorobenzoate
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2008_06
Nc1cc(F)ccc1Br
Reaction #219555
expected product
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2008_06
COC(=O)c1cccc(Cl)c1N
Reaction #219564
expected product
Ausbeute 79.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2008_06
COC(=O)c1c(N)cccc1F
Reaction #219569
methyl 2-amino-6-fluorobenzoate
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2008_06
COc1cc2ncc(=O)[nH]c2cc1OC
Reaction #342506
product
Ausbeute 38.8%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2011_01
CCOC(=O)c1ccc(OCC2CC(O)CN2C(=O)Cc2ccc(NC(=O)Nc3ccccc3C)c(OC)c2)c(OC)c1
Reaction #437564
ethyl 4-[4-hydroxy-1-[3-methoxy-4-[N′-(2-methylphenyl)ureido]phenylacetyl]-2-pyrrolidinylmethoxy]-3-methoxybenzoate
Ausbeute 24.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2007_02
CCOC(=O)c1ccc(OCC2CC(O)CN2C(=O)Cc2ccc(NC(=O)Nc3ccccc3C)c(OC)c2)c(OC)c1
Reaction #441502
ethyl 4-[4-hydroxy-1-[3-methoxy-4-[N′-(2-methylphenyl)ureido]phenylacetyl]-2-pyrrolidinylmethoxy]-3-methoxybenzoate
Ausbeute 24.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2004_06
Cc1ccc(S(=O)(=O)OCC2COc3ccc4ncccc4c3O2)cc1
Reaction #479321
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2004_10
Cc1ccc(S(=O)(=O)OCC2COc3ccc4nc(C)ccc4c3O2)cc1
Reaction #479324
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2004_10
CCc1ccc2c3c(ccc2n1)OCC(COS(=O)(=O)c1ccc(C)cc1)O3
Reaction #479326
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2004_10
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