4-(2-aminoethyl)benzenesulfonamide

NS(=O)(=O)c1ccc(CCNC(C(=O)O)c2c[nH]c3ccccc23)cc1.O
Reaction #5710
title compound
수율 63355.6%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1993_09
NS(=O)(=O)c1ccc(CCNCCCOc2cccc(-c3noc4ccsc34)c2)cc1
Reaction #8752
title compound
수율 35.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
NS(=O)(=O)c1ccc(CCNCc2cccc(-c3cccc(C(=O)NCCN4CCCC4)c3)c2)cc1
Reaction #9870
3′-[{2-[4-(Aminosulfonyl)phenyl]ethyl}aminomethyl]-N-[2-(1-pyrrolidinyl)ethyl]-[1,1′-biphenyl]-3-carboxamide
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
CS(=O)(=O)N(CCCN)Cc1cccc(-c2ccnc(NCCc3ccc(S(N)(=O)=O)cc3)n2)c1
Reaction #42988
4-{2-[4-(3-{[(3-Amino-propyl)-methanesulfonyl-amino]-methyl}-phenyl)-pyrimidin-2-ylamino]-ethyl}-benzenesulfonamide
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
NS(=O)(=O)c1ccc(CCN(Cc2nccc3ccccc23)Cc2nccc3ccccc23)cc1
Reaction #84598
4-(2-(bis(isoquinolin-1-ylmethyl)amino)ethyl)benzenesulfonamide
수율 77.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2016_09
CC(C)(C)OC(=O)Cn1ccnc1CN(CCCC[C@H](NC(=O)N[C@@H](CCC(=O)NCCc1ccc(S(N)(=O)=O)cc1)C(=O)OC(C)(C)C)C(=O)OC(C)(C)C)Cc1nccn1CC(=O)OC(C)(C)C
Reaction #84602
(S)-tert-butyl 6-(bis((1-(2-tert-butoxy-2-oxoethyl)-1H-imidazol-2-yl)methyl)amino)-2-(3-((S)-1-tert-butoxy-1,5-dioxo-5-(4-sulfamoylphenethylamino)pentan-2-yl)ureido)hexanoate
수율 101.8%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2016_09
NS(=O)(=O)c1ccc(CCN(Cc2nccc3ccccc23)Cc2nccc3ccccc23)cc1
Reaction #164791
4-(2-(bis(isoquinolin-1-ylmethyl)amino)ethyl)benzenesulfonamide
수율 77.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_09
CC(C)(C)OC(=O)Cn1ccnc1CN(CCCC[C@H](NC(=O)N[C@@H](CCC(=O)NCCc1ccc(S(N)(=O)=O)cc1)C(=O)OC(C)(C)C)C(=O)OC(C)(C)C)Cc1nccn1CC(=O)OC(C)(C)C
Reaction #164795
(S)-tert-butyl 6-(bis((1-(2-tert-butoxy-2-oxoethyl)-1H-imidazol-2-yl)methyl)amino)-2-(3-((S)-1-tert-butoxy-1,5-dioxo-5-(4-sulfamoylphenethylamino)pentan-2-yl)ureido)hexanoate
수율 101.8%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_09
NS(=O)(=O)c1ccc(CCNC(=O)c2cccc(-c3cnc4c(c3)N(Cc3cc(Cl)ccc3C(F)(F)F)CCN4)c2)cc1
Reaction #174864
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
NS(=O)(=O)c1ccc(CCNC(=O)c2ccc(-c3cnc4c(c3)N(Cc3cc(Cl)ccc3C(F)(F)F)CCN4)cc2)cc1
Reaction #188595
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
CC(C)(C)N1C(=O)C(NCCc2ccc(S(N)(=O)=O)cc2)=C(c2ccccc2)S1(=O)=O
Reaction #205387
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
NS(=O)(=O)c1ccc(CCNCc2cccc(-c3cccc(C(=O)NCCN4CCCC4)c3)c2)cc1
Reaction #225884
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
CCc1nc(C(=O)NCCc2ccc(S(N)(=O)=O)cc2)no1
Reaction #267877
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (6/10)
C[C@]12CCCC[C@@H]1CC[C@@H]1[C@@H]2CC[C@]2(C)[C@@H](NCCc3ccc(S(N)(=O)=O)cc3)CC[C@@H]12.C[C@]12CCCC[C@@H]1CC[C@@H]1[C@@H]2CC[C@]2(C)[C@@H](NCCc3ccc(S(N)(=O)=O)cc3)CC[C@@H]12.O
Reaction #415115
17β-[(2-(4-Aminosulfonylphenyl)ethyl)amino)-5α-androstane Hemihydrate
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1993_12
NS(=O)(=O)c1ccc(CCNC(=O)CCC(=O)O)cc1
Reaction #420295
desired product
수율 92000.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_11
NS(=O)(=O)c1ccc(CCNc2nc3nc(SCc4ccccc4)nc(Cl)c3s2)cc1
Reaction #480373
title compound
수율 78.4%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2004_10
NS(=O)(=O)c1ccc(CCNC(=O)c2sccc2Nc2ccnc3[nH]ccc23)cc1
Reaction #657583
3-(1H-Pyrrolo[2,3-b]pyridin-4-ylamino)-thiophene-2-carboxylic acid [2-(4-sulfamoyl-phenyl)-ethyl]-amide
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2015_05
NS(=O)(=O)c1ccc(CCNC(=O)c2ccc(-c3cnc4c(c3)N(Cc3cc(Cl)ccc3C(F)(F)F)CCN4)cc2)cc1
Reaction #746750
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2011_12
CCc1cc(-c2cncc(C(=O)NCCc3ccc(S(N)(=O)=O)cc3)c2)c(C)[nH]c1=O
Reaction #774768
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (3/10)
CC(=O)Oc1c(C)c(C)c2c(c1C)CCC(C)(C(=O)NS(=O)(=O)c1ccc(CCN)cc1)O2
Reaction #890309
DOI: 10.1039/C8SC04228DTest data from https://doi.org/10.1039/C8SC04228D
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