propane-1-sulfonyl chloride

CCCS(=O)(=O)Nc1nc2nc(N)ncc2cc1-c1c(Cl)cccc1Cl
Reaction #3573
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
CCCOc1ccc(NS(=O)(=O)CCC)cc1-c1nn2c(C3CCCC3)nc(C)c2c(=O)[nH]1
Reaction #11374
2-(2-Propoxy-5-propanesulfonylaminophenyl)-5-methyl-7-cyclopentyl-3H-imidazo[5,1-f][1,2,4]-triazin-4-one
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
CCCS(=O)(=O)Nc1cccc(CCN2CCN(c3cccc4nc(C)ccc34)CC2)c1
Reaction #44085
title compound
Ausbeute 62.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
CCCS(=O)(=O)N1CCC(Nc2ccc(C(=O)c3cc(F)ccc3OC)c(N)n2)CC1
Reaction #58400
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2008_09
CCCS(=O)(=O)NCc1ccc(-c2cc(NC(=O)C3(c4ccc5c(c4)OCO5)CC3)ccc2C)cc1
Reaction #67446
1-(benzo[d][1,3]dioxol-5-yl)-N-(6-methyl-4′-(propylsulfonamidomethyl)biphenyl-3-yl)cyclopropanecarboxamide
Ausbeute 10.5%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_09
CCCS(=O)(=O)Nc1ccc(F)c(C(=O)c2c[nH]c3ncc(Br)cc23)c1F
Reaction #88362
desired compound
Ausbeute 50.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2016_09
CCCS(=O)(=O)N1CCC[C@@H](Nc2nc(-c3c[nH]c4ncc(Cl)cc34)ncc2F)C1
Reaction #162057
desired product
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_09
CCCS(=O)(=O)N1CC(Nc2nc(-c3cn(S(=O)(=O)c4ccc(C)cc4)c4ncc(Cl)cc34)ncc2F)C1
Reaction #162063
desired product
Ausbeute 43.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_09
CCCS(=O)(=O)N1CC[C@H](Nc2nc(-c3c[nH]c4ncc(Cl)cc34)ncc2F)C1
Reaction #162074
410
Ausbeute 36.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_09
CCCS(=O)(=O)NCc1ccc2c(c1)C(Cc1ccccc1)C(NC(=O)OC(C)(C)C)CC2
Reaction #170047
product
Ausbeute 81.2%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_09
CCCS(=O)(=O)NCc1ccc(-c2cc(NC(=O)C3(c4ccc5c(c4)OCO5)CC3)ccc2C)cc1
Reaction #170915
1-(benzo[d][1,3]dioxol-5-yl)-N-(6-methyl-4′-(propylsulfonamidomethyl)biphenyl-3-yl)cyclopropanecarboxamide
Ausbeute 10.5%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_09
—
Reaction #172923
solid
Ausbeute 48.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_09
—
Reaction #172934
solid
Ausbeute 49.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_09
CCCS(=O)(=O)Nc1nn(C(=O)OC(C)(C)C)c2ccc(C3C(C#N)=C(C)NC(C)=C3C#N)cc12
Reaction #187402
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
CCCS(=O)(=O)N(Cc1ccc2ccc(C#N)cc2c1)c1ccc(OC2CCN(C(=O)OC(C)(C)C)CC2)cc1
Reaction #189004
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
CCCS(=O)(=O)Nc1ccc(F)c(Br)c1F
Reaction #189344
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
CCCS(=O)(=O)NC(CCN1CCC(c2cccc(NC(=O)C(C)C)c2)CC1)c1ccccc1
Reaction #195681
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
CCCS(=O)(=O)N1CCC1C(=O)Nc1cc(C(C)(C)C)on1
Reaction #198501
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
CCCS(=O)(=O)NCCCOc1nc(C2CC2)nc(NS(=O)(=O)c2ccc(C(C)C)cn2)c1Oc1ccccc1OC
Reaction #205864
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
CCCS(=O)(=O)N1CCC(Oc2ncnc(Nc3ccc(S(C)(=O)=O)cc3)c2[N+](=O)[O-])CC1
Reaction #212382
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
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