1-Butylimidazole

CCCCn1cc[n+](CC(O)CO)c1.[Cl-]
Reaction #90828
product
Ausbeute 99.1%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2016_09
CCCC[n+]1ccn(CCCc2ccc(OC)cc2)c1.[Br-]
Reaction #93518
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1986_09
CCOC(=O)c1nc2c(s1)CCOc1ccc(C#N)cc1-2
Reaction #171817
9-cyano-4,5-dihydro-6-oxa-3-thia-1-aza-benzo[e]azulene-2-carboxylic acid ethyl ester
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_09
N#Cc1ccc2c(c1)-c1sc(-c3nncn3-c3ccc(F)cc3Cl)cc1CCO2
Reaction #171821
355
Ausbeute 30.3%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_09
CNC(=O)c1cc(C#N)cc(C)c1N
Reaction #245661
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
CNC(=O)c1cc(C#N)cc(C)c1N
Reaction #288236
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (6/10)
N#Cc1ccc([C@]23CN(C(=O)OCc4ccccc4)C[C@H]2CSC(NC(=O)c2ccccc2)=N3)s1
Reaction #425314
title compound
Ausbeute 74.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_11
N#Cc1ccc([C@]23CN(C(=O)OCc4ccccc4)C[C@H]2CSC(NC(=O)c2ccccc2)=N3)s1
Reaction #557437
title compound
Ausbeute 74.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_01
CCOC(=O)c1nc2c(s1)CCOc1ccc(C#N)cc1-2
Reaction #715229
9-cyano-4,5-dihydro-6-oxa-3-thia-1-aza-benzo[e]azulene-2-carboxylic acid ethyl ester
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2016_04
N#Cc1ccc2c(c1)-c1sc(-c3nncn3-c3ccc(F)cc3Cl)cc1CCO2
Reaction #715232
355
Ausbeute 30.3%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2016_04
CCCC[n+]1ccn(CC)c1
Reaction #886472
DOI: 10.1039/C8SC04228DTest data from https://doi.org/10.1039/C8SC04228D
CCCC[n+]1ccn(CCCc2ccc(OC)cc2)c1
Reaction #894874
DOI: 10.1039/C8SC04228DTest data from https://doi.org/10.1039/C8SC04228D
CNC(=O)c1cc(C#N)cc(C)c1N
Reaction #972831
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2012_08
CNC(=O)c1cc(C#N)cc(C)c1N
Reaction #972833
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2012_08
CNC(=O)c1cc(C#N)cc(C)c1N
Reaction #972834
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2012_08
CNC(=O)c1cc(C#N)cc(C)c1N
Reaction #972835
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2012_08
CNC(=O)c1cc(C#N)cc(C)c1N
Reaction #972836
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2012_08
CNC(=O)c1cc(C#N)cc(C)c1N
Reaction #972838
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2012_08
CNC(=O)c1cc(C#N)cc(C)c1N
Reaction #972839
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2012_08
CNC(=O)c1cc(C#N)cc(C)c1N
Reaction #972840
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2012_08
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