5-fluoroisatin

COc1ccc(CN2C(=O)C(=O)c3cc(F)ccc32)cc1
Reaction #43544
5-Fluoro-1-(4-methoxy-benzyl)-1H-indole-2,3-dione
Выход 82.4%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
COc1ccc(CN2C(=O)C(=O)c3cc(F)ccc32)cc1
Reaction #43546
5-Fluoro-1-(4-methoxy-benzyl)-1H-indole-2,3-dione
Выход 80.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
O=C1Cc2cc(F)ccc2N1
Reaction #52585
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2005_02
CNC(=O)N1C(=O)C(=O)c2cc(F)ccc21
Reaction #62830
5-fluoro-1-methylcarbamoylisatin
Выход 74.5%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1988_08
NNC(=O)Cc1cc(F)ccc1N
Reaction #78278
(2-amino-5-fluoro-phenyl)-acetic acid hydrazide
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2004_03
COc1ccc(CN2C(=O)C(=O)c3cc(F)ccc32)cc1
Reaction #174292
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
O=C1C(=O)N(C(c2ccccc2)c2ccccc2)c2ccc(F)cc21
Reaction #176256
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
O=C1C(=O)N(Cc2ccc(C(F)(F)F)o2)c2ccc(F)cc21
Reaction #185758
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
COc1ccc(CN2C(=O)C(=O)c3cc(F)ccc32)cc1
Reaction #219303
5-Fluoro-1-(4-methoxy-benzyl)-1H-indole-2,3-dione
Выход 82.4%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2008_06
COc1ccc(CN2C(=O)C(=O)c3cc(F)ccc32)cc1
Reaction #219309
5-Fluoro-1-(4-methoxy-benzyl)-1H-indole-2,3-dione
Выход 80.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2008_06
O=C1Cc2cc(F)ccc2N1
Reaction #296646
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (6/10)
O=C1c2cc(F)ccc2-n2c1nc1ccc(Cl)cc1c2=O
Reaction #302976
2-Chloro-8-fluoroindolo[2,1-b]quinazoline-6,12-dione
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2012_06
O=C(O)c1c(O)c(-c2ccccc2)nc2ccc(F)cc12
Reaction #316039
6-fluoro-3-hydroxy-2-phenyl-quinoline-4-carboxylic acid
Выход 21.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2009_07
O=C(O)c1c(O)c(-c2ccc(-c3ccccc3)cc2)nc2ccc(F)cc12
Reaction #318835
desired product
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1989_07
NC(=O)CCN1C(=O)C(=O)c2ccccc21
Reaction #321471
5-fluoroisatin acetamide
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1997_01
Nc1ccc(F)cc1C(=O)O
Reaction #325408
2-amino-5-fluoro-benzoic acid
Выход 80.9%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_02
Cc1c(-c2cccc(C(F)(F)F)c2)nc2ccc(F)cc2c1C(=O)O
Reaction #332402
6-fluoro-3-methyl-2-[3-(trifluoromethyl)phenyl]-4-quinolinecarboxylic acid
Выход 91.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_02
Cc1c(-c2cccc(C(F)(F)F)c2)nc2ccc(F)cc2c1C(=O)O
Reaction #332411
6-fluoro-3-methyl-2-[3-(trifluoromethyl)phenyl]-4-quinolinecarboxylic acid
Выход 100.2%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_02
Cc1c(-c2cccc(Br)c2)nc2ccc(F)cc2c1C(=O)O
Reaction #332433
2-(3-bromophenyl)-6-fluoro-3-methyl-4-quinolinecarboxylic acid
Выход 98.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_02
Cc1ccccc1-c1ccc2c(c1)CCCc1c-2nc2ccc(F)cc2c1C(=O)O
Reaction #351947
above-mentioned compound
Выход 48.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1997_07
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