3-fluoropyridine-4-carboxylic acid

O=C(O)c1ccncc1Nc1ccc(Cl)cc1Cl
Reaction #67777
desired product
Rendimiento 72.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_09
Cc1cc(Br)ccc1Nc1cnccc1C(=O)O
Reaction #67778
desired product
Rendimiento 70.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_09
Cc1cc(I)ccc1Nc1cnccc1C(=O)O
Reaction #67779
desired product
Rendimiento 59.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_09
O=C(O)c1cc[n+]([O-])cc1F
Reaction #67786
3-fluoroisonicotinic acid 1-oxide
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_09
O=C(O)c1ccncc1Nc1ccc(I)cc1Cl
Reaction #67796
3-[(2-chloro-4-iodophenyl)amino]isonicotinic acid
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_09
COc1ccc(Nc2cnccc2C(=O)O)cc1
Reaction #67878
desired product
Rendimiento 13.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_09
O=C(O)c1ccncc1Nc1ccc(SC(F)(F)F)cc1
Reaction #67879
desired product
Rendimiento 10.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_09
O=C(O)c1ccncc1Nc1ccc(OC(F)(F)F)cc1
Reaction #67880
desired product
Rendimiento 9.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_09
O=C(OC1CCC(Oc2ccc3c(c2)CCC(c2ccccc2)O3)CC1)c1ccncc1F
Reaction #88058
title compound
Rendimiento 68.4%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2016_09
O=C(O)c1ccncc1NCc1ccccc1F
Reaction #91310
title compound
Rendimiento 10.3%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2016_09
O=C(O)c1ccncc1NCc1cccc(F)c1
Reaction #91311
title compound
Rendimiento 33.2%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2016_09
N#Cc1ccc(CNc2cnccc2C(=O)O)cc1
Reaction #91314
title compound
Rendimiento 18.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2016_09
COc1ccc(CNc2cnccc2C(=O)O)cc1
Reaction #91316
title compound
Rendimiento 26.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2016_09
O=C(O)c1ccncc1NCc1ccc(C(F)(F)F)cc1
Reaction #91317
title compound
Rendimiento 28.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2016_09
O=C(O)c1ccncc1NCc1ccc(-c2ccccc2)cc1
Reaction #91319
title compound
Rendimiento 36.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2016_09
O=C(O)c1ccncc1NCc1ccc(Cl)cc1
Reaction #91320
title compound
Rendimiento 32.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2016_09
CC(C)Oc1ccc(CNc2cnccc2C(=O)O)cc1
Reaction #91322
title compound
Rendimiento 28.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2016_09
O=C(O)c1ccncc1NCc1ccc(Oc2ccccc2)cc1
Reaction #91323
title compound
Rendimiento 36.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2016_09
O=C(O)c1ccncc1NCc1ccc(Cl)c(Cl)c1
Reaction #91325
title compound
Rendimiento 37.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2016_09
Cc1cc(Cl)ccc1CNc1cnccc1C(=O)O
Reaction #91327
title compound
Rendimiento 45.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2016_09
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