1,2-Dimethylimidazole

Cn1ccnc1-c1cnc(NCCNc2ccc([N+](=O)[O-])cn2)nc1-c1ccc(Cl)cc1Cl
Reaction #60152
[4-(2,4-dichlorophenyl)-5-(1-methylimidazol-2-yl)pyrimidin-2-yl]{2-[(5-nitro(2-pyridyl))amino]ethyl}amine
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2008_09
Cn1ccnc1-c1cnc(NCCNc2ccc(C#N)cn2)nc1-c1ccc(Cl)cc1Cl
Reaction #60156
6-[(2-{[4-(2,4-dichlorophenyl)-5-(1-methylimidazol-2-yl)pyrimidin-2-yl]amino}-ethyl)amino]pyridine-3-carbonitrile
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2008_09
Cn1ccnc1-c1cnc(NCCNc2ccc(C(F)(F)F)cn2)nc1-c1ccc(Cl)cc1Cl
Reaction #60157
[4-(2,4-dichlorophenyl)-5-(1-methylimidazol-2-yl)pyrimidin-2-yl](2-{[5-(trifluoromethyl)(2-pyridyl)]amino}ethyl)amine
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2008_09
Cc1n(C)cc[n+]1CC(O)CO.[Cl-]
Reaction #90825
solid
Ausbeute 100.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2016_09
—
Reaction #93525
monohydrate
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1986_09
CCc1nn(Cc2cccc(C)n2)c2cccc(NC(=O)c3cnc4cc(-c5cnc(C)n5C)ccn34)c12
Reaction #166542
final product
Ausbeute 15.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_09
Cc1ccsc1C=Cc1nccn1C
Reaction #266226
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (6/10)
Cc1ccsc1C=Cc1nccn1C
Reaction #458895
1-methyl-2-(2-(3-methyl-2-thienyl)ethenyl)1H-imidazole
Ausbeute 41.2%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1978_05
CC1N(C)C=C[NH+]1C.[I-]
Reaction #522751
1,2,3-trimethyl-1H-imidazolium iodide
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1977_02
CCCn1cc[n+](C)c1C.[I-]
Reaction #536424
1,2-dimethyl-3-propylimidazolium iodide
Ausbeute 92.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_07
COc1nc(-c2cnc(C)n2C)ccc1N
Reaction #610280
title compound
Ausbeute 16.5%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2016_05
—
Reaction #610281
solid
Ausbeute 15.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2016_05
CCCCCCCCCCCCCCCCn1cc[n+](C)c1C.[Cl-]
Reaction #693738
1,2-dimethyl-3-hexadecylimidazolium chloride
Ausbeute 62.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2011_03
Cc1ncc(-c2cnc(N3CCc4c([nH]c5ccccc45)C3c3ccc4c(c3)CCO4)nc2)n1C
Reaction #1070601
title product
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2005_03
Cc1ncc(-c2cnc(N3CCc4c([nH]c5ccccc45)C3c3ccc4c(c3)CCO4)nc2)n1C
Reaction #1075512
title product
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2003_10
Cc1n(C(=O)C2C(C)(C)C2(C)C)cc[n+]1C.[Cl-]
Reaction #1269217
Intermediate 25
Ausbeute 84.5%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2007_10
Cc1ncc(-c2cnc(N3CCc4c([nH]c5ccccc45)C3c3ccc4c(c3)CCO4)nc2)n1C
Reaction #1311064
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (5/10)
Cc1n(CC(=O)N2CCCC2)cc[n+]1C.[Cl-]
Reaction #1462117
white solid
Ausbeute 41.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2007_01
Cc1n(C)cc[n+]1CCCCc1ccc(Cl)cc1.[Cl-]
Reaction #1467538
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1986_04
Cc1n(C)cc[n+]1CC(O)CO.[Cl-]
Reaction #1509602
solid
Ausbeute 100.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2015_01
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