2-fluorobenzoic acid

Cc1ccc2c(N3CCN(CC(C)c4cccc(NC(=O)c5ccccc5F)c4)CC3)cccc2n1
Reaction #44127
title compound
Ausbeute 64.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
CCCCc1nn(-c2cc(NC(=O)CC)ccc2C(F)(F)F)c(=O)n1Cc1ccc(-c2ccccc2S(=O)(=O)NC(=O)c2ccccc2F)cc1F
Reaction #64584
title compound
Ausbeute 93.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1995_05
O=C(NCc1cc(-c2nn(-c3ccc(Cl)cc3)c(=O)[nH]2)c(Cl)cc1F)c1ccccc1F
Reaction #87815
desired product
Ausbeute 9.5%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2016_09
O=C(SCC1C(=O)OCC1c1ccccc1)c1ccccc1F
Reaction #93540
title compound
Ausbeute 67.2%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1986_09
CCN(CC(O)(CNc1cc(C)cc2c1cnn2-c1ccc(F)cc1)C(F)(F)F)C(=O)c1ccccc1F
Reaction #185179
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
CC(C)N(c1ccccc1C(=O)O)C(C)C
Reaction #191747
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
CCOC(=O)CC(=O)c1ccccc1F
Reaction #193658
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
O=C(O)c1ccccc1F
Reaction #198687
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
O=C(Cl)c1ccccc1F
Reaction #199896
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
O=C(SCC1C(=O)OCC1c1ccccc1)c1ccccc1F
Reaction #209252
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
O=C(Nc1c[nH]nc1C(=O)Nc1ccc(F)cc1)c1ccccc1F
Reaction #219211
product
Ausbeute 19.1%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2008_06
CC(C)(C)c1nc(C2CCC2)cc(N2CCN(CCCCNC(=O)c3ccccc3F)CC2)n1
Reaction #236442
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
O=C(O)c1ccccc1F
Reaction #247285
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
O=C(O)c1ccccc1F
Reaction #251274
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
Cc1ccc2c(N3CCN(CC(C)c4cccc(NC(=O)c5ccccc5F)c4)CC3)cccc2n1
Reaction #267676
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (6/10)
Cc1ccccc1-c1c(C(=O)O)ccc2ccccc12
Reaction #267677
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (6/10)
CCOC(=O)C(OC(=O)c1ccccc1F)C(=O)c1ccccc1
Reaction #272716
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (6/10)
CN(Cc1ccccc1)c1ccccc1C(=O)O
Reaction #287958
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (6/10)
CCCN(CC(O)(CNc1cccc2c1cnn2-c1ccc(F)cc1)C(F)(F)F)C(=O)c1ccccc1F
Reaction #291271
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (6/10)
CC(C)(C)c1nc(C2CCC2)cc(N2CCN(CCCCNC(=O)c3ccccc3F)CC2)n1
Reaction #306913
title compound
Ausbeute 88.5%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2012_06
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