4-Methyl-1H-imidazole

Cc1cn(-c2ccc([N+](=O)[O-])cc2F)cn1
Reaction #8251
3-Fluoro-4-(4-methylimidazol-1-yl)nitrobenzene
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
Cc1cn(-c2cnc3nnn(Cc4ccc5ncccc5c4)c3n2)cn1
Reaction #44268
6-((6-(4-methyl-1H-imidazol-1-yl)-1H-[1,2,3]triazolo[4,5-b]pyrazin-1-yl)methyl)quinoline
Ausbeute 56.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
Cc1cn(-c2ccc(C=O)cc2F)cn1
Reaction #44606
title compound
Ausbeute 17.6%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
Cc1cncn1Cc1ccc([N+](=O)[O-])cc1
Reaction #58972
5-methyl-1-(4-nitrobenzyl)-1H-imidazole
Ausbeute 3.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2008_09
Cc1c[nH]c(CC(=O)c2ccc(Cl)cc2Cl)n1
Reaction #60199
1-(2,4-Dichlorophenyl)-2-(4-methylimidazolyl)ethan-1-one
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2008_09
Cc1cn(-c2ccc(S(C)(=O)=O)cc2C(=O)N2CCN(c3ccc(C(F)(F)F)cc3)CC2)cn1
Reaction #61041
title compound
Ausbeute 32.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2008_09
Cc1cn(-c2cc(F)c([C@H](C)N)cc2F)cn1
Reaction #85724
(S)-1-(2,5-difluoro-4-(4-methyl-1H-imidazol-1-yl)phenyl)ethanamine
Ausbeute 143.4%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2016_09
Cc1cn(-c2cc(N)cc(C(F)(F)F)c2)cn1
Reaction #167781
desired product
Ausbeute 91.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_09
Cc1cncn1-c1ccc(Br)cc1C#N
Reaction #175925
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
Cc1cn(-c2sccc2[N+](=O)[O-])cn1
Reaction #178314
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
Cc1cn(-c2ccc([N+](=O)[O-])cc2C#N)cn1
Reaction #198581
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
COc1cc([N+](=O)[O-])ccc1-n1cnc(C)c1
Reaction #204334
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
CCOC(=O)Cn1cnc(C)c1
Reaction #205271
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
Cc1cn(C(c2ccccc2)(c2ccccc2)c2ccccc2)cn1
Reaction #221859
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
COc1ccc2c(-n3cnc(C)c3)nc(C#N)c(Cl)c2c1
Reaction #243114
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
Cc1cn(-c2ccc([N+](=O)[O-])cc2C#N)cn1
Reaction #243559
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
CC(=O)n1cnc(C)c1
Reaction #248936
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
Cc1nc[nH]c1CSCCN
Reaction #267802
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (6/10)
CCOc1cc(C=O)ccc1-n1cnc(C)c1
Reaction #275453
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (6/10)
CCOC(=O)Cn1cnc(C)c1
Reaction #329437
(4-Methyl-1H-imidazol-1-yl)acetic acid ethyl ester
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_02
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