172 件の反応に参加

13625

COC(=O)c1ccc(CNc2cccc3cccnc23)cc1
Reaction #11950
title compound
収率 172.4%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
FC(F)(F)c1ccc2[nH]c(Nc3cccc4cccnc34)nc2c1
Reaction #61826
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2008_09
CC(Nc1cccc2cccnc12)c1ccccc1
Reaction #69597
title compound
収率 91.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_09
Cc1ccccc1C(Nc1cccc2cccnc12)c1ccccc1
Reaction #69601
N-[(2-Methylphenyl)(phenyl)methyl]quinolin-8-amine
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_09
O=C(CC1CCc2cc(Br)cc3[nH]c(=O)c(=O)n1c23)Nc1cccc2cccnc12
Reaction #80833
title compound
収率 77.4%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1997_04
CCn1nc(-c2cccc(Cl)c2)c(C(C)=O)c(Nc2cccc3cccnc23)c1=O
Reaction #178326
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
C=CC(=O)Nc1cccc2cccnc12
Reaction #192316
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
O=C1CCCN1c1cccc2cccnc12
Reaction #208000
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
CC(Nc1cccc2cccnc12)c1ccccc1
Reaction #212476
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
Nc1cccc2c(Cl)ccnc12
Reaction #218363
8-amino-4-chloro-quinoline
収率 34.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2008_06
O=C(CC1CCc2cc(Br)cc3[nH]c(=O)c(=O)n1c23)Nc1cccc2cccnc12
Reaction #225378
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
Nc1ccc(Br)c2cccnc12
Reaction #235043
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
CC(C)(C)c1ccc(Nc2cccc3cccnc23)cc1
Reaction #239326
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
CCCCS(=O)(=O)Nc1cccc2cccnc12
Reaction #242989
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
COC(=O)c1ccc(CNc2cccc3cccnc23)cc1
Reaction #245365
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
Nc1cccc2c(Cl)ccnc12
Reaction #248303
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
CS(=O)(=O)Nc1cccc2cccnc12
Reaction #251801
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
O=C(Nc1cccc2cccnc12)C(Cl)(Cl)Cl
Reaction #272541
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (6/10)
COc1cc2ncc(C#N)c(Nc3cccc4cccnc34)c2cc1OC
Reaction #277293
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (6/10)
Cc1ccccc1C(Nc1cccc2cccnc12)c1ccccc1
Reaction #286563
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (6/10)
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