#11206379

O=Cc1cc2cccc(Cl)c2nc1-c1ccccc1C(F)(F)F
Reaction #279818
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (6/10)
O=Cc1cc2cccc(Cl)c2nc1-c1ccccc1Cl
Reaction #303927
8-chloro-2-(2-chlorophenyl)quinoline-3-carbaldehyde
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2012_06
O=C1c2ccccc2C(=O)N1Cc1cc2cccc(Cl)c2nc1Cl
Reaction #303958
2-((2,8-Dichloroquinolin-3-yl)methyl)isoindoline-1,3-dione
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2012_06
O=Cc1cc2cccc(Cl)c2nc1Oc1ccccc1
Reaction #303964
8-chloro-2-phenoxyquinoline-3-carbaldehyde
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2012_06
CC(C)(C)[S@@](=O)/N=C/c1cc2cccc(Cl)c2nc1Cl
Reaction #329323
title compound
收率 97.5%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_02
CC(C)(C)[S@@](=O)/N=C/c1cc2cccc(Cl)c2nc1Cl
Reaction #562221
title compound
收率 97.5%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_01
O=Cc1cc2cccc(Cl)c2nc1-c1cccnc1
Reaction #659300
title compound
收率 91.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2015_05
O=Cc1cc2cccc(Cl)c2nc1-c1ccccc1
Reaction #659306
title compound
收率 97.1%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2015_05
O=Cc1cc2cccc(Cl)c2nc1-c1cnccn1
Reaction #659307
title compound
收率 99.8%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2015_05
COc1cncc(-c2nc3c(Cl)cccc3cc2C=O)n1
Reaction #659308
title compound
收率 63.4%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2015_05
O=Cc1cc2cccc(Cl)c2nc1-c1ccc(Cl)nc1
Reaction #659318
title compound
收率 123.3%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2015_05
CC(C)(C)S(=O)N=Cc1cc2cccc(Cl)c2nc1Cl
Reaction #900759
DOI: 10.1039/C8SC04228DTest data from https://doi.org/10.1039/C8SC04228D
O=Cc1cc2cccc(Cl)c2nc1-c1ccccc1Cl
Reaction #1484840
8-chloro-2-(2-chlorophenyl)quinoline-3-carbaldehyde
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_12
NCc1cc2cccc(Cl)c2nc1-c1ccccn1
Reaction #1484869
(8-chloro-2-(pyridin-2-yl)quinolin-3-yl)methanamine
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_12
O=Cc1cc2cccc(Cl)c2nc1Oc1ccccc1
Reaction #1484875
8-chloro-2-phenoxyquinoline-3-carbaldehyde
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_12
O=Cc1cc2cccc(Cl)c2nc1-c1ccccc1Cl
Reaction #1622410
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (1/10)
CC(C)(C)[S@@](=O)/N=C/c1cc2cccc(Cl)c2nc1Cl
Reaction #1714685
title compound
收率 97.5%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_07
CC(C)(C)[S@@](=O)/N=C/c1cc2cccc(Cl)c2nc1Cl
Reaction #1937989
title compound
收率 97.5%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2015_02
CC(C)(C)[S@@](=O)/N=C/c1cc2cccc(Cl)c2nc1Cl
Reaction #1981853
title compound
收率 97.5%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_08
O=Cc1cc2cccc(Cl)c2nc1-c1ccccc1Cl
Reaction #2132004
8-chloro-2-(2-chlorophenyl)quinoline-3-carbaldehyde
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_11
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