5-amino-2-fluorobenzonitrile

Cc1nn(-c2ccc(F)c(C#N)c2)c2c1CCN(c1ccc(Br)cc1)C2=O
Reaction #53448
1-[3-cyano-4-fluorophenyl]-3-methyl-6-[4-bromophenyl]-1,4,5,6-tetrahydro-7H-pyrazolo[3,4-c]pyridin-7-one
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2005_02
COCCNc1nonc1C(=NO)Nc1ccc(F)c(C#N)c1
Reaction #156984
desired compound
Выход 100.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_09
CS(=O)(=O)NCCNc1nonc1C(=NO)Nc1ccc(F)c(C#N)c1
Reaction #156986
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_09
N#Cc1cc(N)ccc1F
Reaction #384210
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (8/10)
N#Cc1cc(N)ccc1F
Reaction #463611
2-fluoro-5-aminobenzonitrile
Выход 85.7%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2000_02
COCCNc1nonc1C(=NO)Nc1ccc(F)c(C#N)c1
Reaction #503026
desired compound
Выход 100.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2012_01
CS(=O)(=O)NCCNc1nonc1C(=NO)Nc1ccc(F)c(C#N)c1
Reaction #503028
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2012_01
N#Cc1cc(NC(=O)N2CCc3ccccc3[C@H]2c2ccc(C(F)(F)F)cc2)ccc1F
Reaction #532522
desired product
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_07
COc1ccc(C(=O)Nc2ccc(F)c(CNc3ncnc4c(C(N)=O)cccc34)c2)cc1
Reaction #665891
4-[2-Fluoro-5-(4-methoxy-benzoylamino)-benzylamino]-quinazoline-8-carboxylic acid amide
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2015_05
N#Cc1cc(N)ccc1F
Reaction #701693
3-cyano-4-fluoroaniline
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1979_03
COCCNc1nonc1C(=NO)Nc1ccc(F)c(C#N)c1
Reaction #718324
desired compound
Выход 100.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2016_04
CS(=O)(=O)NCCNc1nonc1C(=NO)Nc1ccc(F)c(C#N)c1
Reaction #718326
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2016_04
N#Cc1cc(N)ccc1F
Reaction #775716
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (3/10)
N#Cc1cc(NC(=O)Cc2nc(N3CCOCC3)cc(=O)[nH]2)ccc1F
Reaction #967259
N-(3-cyano-4-fluorophenyl)-2-[4-(morpholin-4-yl)-6-oxo-1,6-dihydropyrimidin-2-yl]acetamide
Выход 22.7%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2015_03
COCCNc1nonc1C(=NO)Nc1ccc(F)c(C#N)c1
Reaction #968361
desired compound
Выход 100.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2015_03
CS(=O)(=O)NCCNc1nonc1C(=NO)Nc1ccc(F)c(C#N)c1
Reaction #968363
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2015_03
N#Cc1cc(N)ccc1F
Reaction #1055525
4-fluoro-3-cyanoaniline
Выход 85.4%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2005_10
N#Cc1cc(N)ccc1F
Reaction #1055540
5-amino-2-fluorobenzonitrile
Выход 99.7%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2005_10
N#Cc1cc(N)ccc1F
Reaction #1150669
4-fluoro-3-cyanoaniline
Выход 85.4%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2005_11
N#Cc1cc(N)ccc1F
Reaction #1158650
4-fluoro-3-cyanoaniline
Выход 85.4%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2005_06
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