4-cyanobenzyl bromide

N#Cc1ccc(CN=[N+]=[N-])cc1
Reaction #951
4-cyanobenzyl azide
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
N#Cc1ccc(CN2CCN(Cc3ccc(C#N)cc3)C2=O)cc1
Reaction #1695
4,4'-[(2-oxoimidazolin-1,3-diyl)bis(methylene)]-bis(benzonitrile)
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
N#Cc1ccc(CN2CCN(Cc3ccc(C#N)cc3)C2=O)cc1
Reaction #1760
4,4'-[(2-oxoimidazolin-1,3-diyl)bis(methylene)]-bis(benzonitrile)
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
N#Cc1ccc(CN2CCN(Cc3ccc(C#N)cc3)C2=O)cc1
Reaction #2230
4,4'-[(2-oxoimidazolin-1,3-diyl) bis(methylene)]-bis(benzonitrile)
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
N#Cc1ccc(CN2CCN(Cc3ccc(C#N)cc3)C2=O)cc1
Reaction #2794
4,4'-[(2-oxoimidazolin-1,3-diyl)bis(methylene)]-bis(benzonitrile)
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
N#Cc1ccc(CN2CCN(Cc3ccc(C#N)cc3)C2=O)cc1
Reaction #2818
4,4'-[(2-oxoimidazolin-1,3-diyl)bis(methylene)]-bis(benzonitrile)
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
N#Cc1ccc(CN([C@H]2CCCC[C@H]2C(N)=O)S(=O)(=O)c2ccc(Cl)cc2)cc1
Reaction #7135
titled compound
Ausbeute 49.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
N#Cc1ccc(CN([C@@H]2CCCC[C@H]2C(N)=O)S(=O)(=O)c2ccc(Cl)cc2)cc1
Reaction #7139
titled compound
Ausbeute 43.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
N#Cc1ccc(CN([C@H]2CCCCC[C@H]2C(N)=O)S(=O)(=O)c2ccc(Cl)cc2)cc1
Reaction #7141
titled compound
Ausbeute 3.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
N#Cc1ccc(CN([C@H]2CCC[C@H]2C(N)=O)S(=O)(=O)c2ccc(Cl)cc2)cc1
Reaction #7146
titled compound
Ausbeute 20.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
CCCc1nc2cc(N(Cc3ccc(C#N)cc3)S(=O)(=O)c3ccc(F)cc3)ccc2n1CC(=O)OC(C)(C)C
Reaction #43842
{5-[(4-Cyano-benzyl)-(4-fluoro-benzenesulfonyl)-amino]-2-propyl-benzoimidazol-1-yl}-acetic acid tert-butyl ester
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
N#Cc1ccc(CO)cc1
Reaction #44329
4-cyanobenzyl alcohol
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
CC(C)c1cc(OCc2ccc(C#N)cc2)nc(-c2cc(Cl)cc(Cl)c2)n1
Reaction #58184
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2008_09
N#Cc1ccc(COc2nc(-c3cc(Cl)cc(Cl)c3)nc3c2CN(Cc2ccccc2)CC3)cc1
Reaction #58185
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2008_09
CC(C)c1cc(OCc2ccc(C#N)cc2)nc(-c2cccc([N+](=O)[O-])c2)n1
Reaction #58186
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2008_09
N#Cc1ccc(COc2nc(-c3cccc([N+](=O)[O-])c3)nc3c2CN(Cc2ccccc2)CC3)cc1
Reaction #58187
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2008_09
CCC(=O)C(Cc1ccc(C#N)cc1)C(=O)CC
Reaction #59434
title compound
Ausbeute 58.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2008_09
N#Cc1ccc(Cc2ncc[nH]2)cc1
Reaction #64183
4-[1-(imidazolyl)methyl]benzonitrile
Ausbeute 71.9%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1995_05
N#Cc1ccc(Cc2nc[nH]n2)cc1
Reaction #64190
4-[1-(1,2,4-triazolyl)methyl]benzonitrile
Ausbeute 67.5%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1995_05
N#Cc1ccc(CN=[N+]=[N-])cc1
Reaction #64198
4-azidomethylbenzonitrile
Ausbeute 96.7%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1995_05
Seite 1Weiter