Involved in 67 reactions

6830

NCCCC1CCCc2cccnc21
Reaction #4605
3-(5,6,7,8-tetrahydroquinol-8-yl)propylamine
Yield 26.5%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1988_02
NCCCC1CCCc2cccnc21
Reaction #63198
3-(5,6,7,8-tetrahydroquinol-8-yl) propylamine
Yield 26.5%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1988_08
ClCCCN=Cc1ccncc1
Reaction #320712
Pyridine-4-carboxaldehyde (3-Chloropropyl)imine
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1997_01
ClCCCN=Cc1ccncc1
Reaction #320741
Pyridine-4-carboxaldehyde (3-Chloropropyl)imine
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1997_01
O=S(=O)(NCCCCl)c1ccc(Nc2ncnc3cc(Cl)ccc23)cc1
Reaction #322837
title compound
Yield 60.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1987_02
ClCCCN=Cc1ccncc1
Reaction #412282
Pyridine-4-carboxaldehyde (3-Chloropropyl)imine
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2001_04
CCc1nn(CCCN)c(CC)c1Cc1cc(Cl)cc(Cl)c1
Reaction #440263
title compound
Yield 84.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2004_06
Cc1cccnc1CCCCN
Reaction #457701
4-(3-methyl-2-pyridyl) butylamine
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1985_07
O=C(NCCCCl)Oc1ccccc1
Reaction #475065
title compound
Yield 40.4%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_02
Cc1cccnc1CCCCN
Reaction #549680
4-(3-methyl-2-pyridyl)butylamine
Yield 62.3%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1985_05
Cn1cc(NC(=O)Nc2ccc(OC(F)(F)F)cc2)nc1C(=O)NCCCCl
Reaction #587106
N-(3-Chloropropyl)-1-methyl-4-[({[4-(trifluoromethoxy)phenyl]amino}carbonyl)amino]-1H-imidazol-2-carboxamide
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_08
CCCCCCNC(=O)NCCCCl
Reaction #630366
1-(3-chloropropyl)-3-n-hexylurea
Yield 86.1%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1987_04
N#Cc1ccc(NC(=O)NCCCCl)cc1
Reaction #630370
1-(3-chloropropyl)-3-(4-cyanophenyl)urea
Yield 54.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1987_04
ClCCCNCc1ccc(Cl)nc1
Reaction #640093
3-chloro-N-[(6-chloropyridin-3-yl)methyl]propan-1-amine
Yield 87.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2011_05
CC(=O)N1CCCC2=C1CCc1cc(Cl)ccc12
Reaction #656833
4-acetyl-8-chloro-1,2,3,4,5,6-hexahydrobenzo[f]quinoline
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1988_03
O=S(=O)(NCCCCl)c1ccc(Nc2ncnc3cc(Cl)ccc23)cc1
Reaction #657239
title compound
Yield 60.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1988_03
CCc1nn(CCCN)c(CC)c1Cc1cc(Cl)cc(Cl)c1
Reaction #810787
title compound
Yield 84.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_11
CCc1onc(-c2ccccc2)c1C(=O)NCCCCl
Reaction #927309
title compound
Yield 80.2%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2002_04
CCSCCSCCCN
Reaction #935972
1-amino-4,7-dithianonane
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1981_10
O=C(NCCCCl)Oc1ccccc1
Reaction #940587
title compound
Yield 40.4%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2007_08
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