Участвует в 538 реакциях

79404

Cc1ccccc1-c1ncc(C(=O)N2CCN(C(C)C)CC2)n1C
Reaction #40727
(4-isopropyl-piperazin-1-yl)-(3-methyl-2-o-tolyl-3H-imidazol-4-yl)-methanone
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
COc1ncc(-c2ccccc2C)c(OC)n1
Reaction #40961
title compound
Выход 46.3%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
Cc1ccccc1-c1ccccn1
Reaction #42149
2-ortho-tolylpyridine
Выход 84.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
Cc1ccccc1-c1ccccn1
Reaction #42166
2-ortho-tolylpyridine
Выход 80.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
Cc1ccccc1N1CCc2ncnc(Nc3ccc(C(F)(F)F)cc3)c2C1
Reaction #47916
desired compound
Выход 5.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
Cc1ccccc1-c1cc(N2CCSCC2)ncc1NC(=O)C(C)(C)C
Reaction #50922
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2005_02
C=CCSCC1=CC(C)(C)Nc2ccc(-c3ccccc3C)cc21
Reaction #54077
4-allylsulfanylmethyl-2,2-dimethyl-6-o-tolyl-1,2-dihydroquinoline
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2005_02
Cc1ccccc1-c1ccc(C=O)c(OCCN(C)C)c1
Reaction #58896
3-(2-Dimethylamino-ethoxy)-2′-methyl-biphenyl-4-carbaldehyde
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2008_09
CCOC(=O)C1(c2ccc(-c3ccc(-c4onc(C)c4Nc4cccc(-c5ccccc5C)n4)cc3)cc2)CC1
Reaction #73881
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_09
Cc1ccccc1-c1ccc2c(c1)OCCC2=O
Reaction #91917
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2016_09
Cc1ccccc1-c1ccc2nc(Cl)c(CO)cc2c1
Reaction #156255
(2-chloro-6-o-tolylquinolin-3-yl)methanol
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_09
Cc1ccccc1-c1ccc2nc(N)c(CC(C)c3cc(CC(C)(C)C)ncn3)cc2c1
Reaction #156265
3-(2-(6-neopentylpyrimidin-4-yl)propyl)-6-o-tolylquinolin-2-amine
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_09
Cc1ccccc1Oc1ccc(-c2cc(C3CCCC3)nc(Cl)c2C#N)cc1
Reaction #168196
2-chloro-6-cyclopentyl-4-(4-(o-tolyloxy)phenyl)nicotinonitrile
Выход 58.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_09
Cc1cc(C)c(CNC(=O)c2cc(-c3ccccc3C)cc3c2cnn3C(C)C)c(=O)[nH]1
Reaction #172708
title compound
Выход 67.6%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_09
Cc1ccccc1-c1ccc([N+](=O)[O-])cc1N
Reaction #176697
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
Cc1ccccc1-c1cccc(C(O)(c2cn(C(c3ccccc3)(c3ccccc3)c3ccccc3)cn2)C(C)C)c1
Reaction #180009
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
Cc1ccccc1-c1ccc(C(=O)c2ccccc2)cc1
Reaction #180277
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
COc1ccc([N+](=O)[O-])c(OC)c1-c1ccccc1C
Reaction #182161
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
Cc1ccccc1-c1cc(N2CCOCC2)ncc1NC(=O)C(C)(C)C
Reaction #187163
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
Cc1ccccc1-c1nc(C)c2c(C)nc3ccc(F)cc3n12
Reaction #190204
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
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