An 57 Reaktionen beteiligt

1306931

CC(C)(C)OC(=O)NC1CN(Cc2cccc(F)c2F)CCN(CC(F)(F)F)C1=O
Reaction #48457
title compound
Ausbeute 88.6%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
O=C1CC(c2cccc(F)c2F)Oc2ccc(O)cc21
Reaction #59574
2-(2,3-Difluorophenyl)-6-hydroxychroman-4-one
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2008_09
Fc1cccc(CNC2CC2)c1F
Reaction #61345
Cyclopropyl-(2,3-difluorobenzyl)amine
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2008_09
CC(C)(C)[S@@](=O)/N=C/c1cccc(F)c1F
Reaction #85733
(R,E)-N-(2,3-difluorobenzylidene)-2-methylpropane-2-sulfinamide
Ausbeute 93.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2016_09
Fc1cccc(CNc2cccc(-c3c(Cc4ccccc4)cnc4c(C(F)(F)F)cccc34)c2)c1F
Reaction #244787
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
CCOC(=O)c1cc(N=Cc2cccc(F)c2F)cn1S(C)(=O)=O
Reaction #288534
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (6/10)
O=C1CC(c2cccc(F)c2F)Oc2ccc(O)cc21
Reaction #377308
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (8/10)
Fc1cccc(CNC2CC2)c1F
Reaction #385894
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (8/10)
O=Cc1cc(Br)cc(F)c1F
Reaction #390354
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (8/10)
O=C(C=Cc1cccc(F)c1F)C=Cc1cccc(F)c1F
Reaction #519967
yellow powder
Ausbeute 4.2%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2003_12
CCCC1=C(C(=O)OCC)C(c2cccc(F)c2F)c2c[nH]nc2N1
Reaction #576522
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2005_12
N#Cc1ccccc1N1CCN(C(=O)C2CC(N(Cc3ccc(F)cc3F)C(=O)OCC(Cl)(Cl)Cl)CN2Cc2cccc(F)c2F)CC1
Reaction #577808
{1-(2,3-Difluoro-benzyl)-5-[4-(2-cyano-phenyl)-piperazine-1-carbonyl]-pyrrolidin-3-yl}-(2,4-difluoro-benzyl)-carbamic acid 2,2,2-trichloro-ethyl ester
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2009_05
CC(C)(C)OC(=O)NC1CN(Cc2cccc(F)c2F)CCN(CC(F)(F)F)C1=O
Reaction #580872
title compound
Ausbeute 88.6%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2009_05
CC(C)(C)OC(=O)NC1CN(Cc2cccc(F)c2F)CCN(CC(F)(F)F)C1=O
Reaction #588353
title compound
Ausbeute 88.6%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_08
COC(=O)[C@H](Cc1ccc(OCCc2nc(-c3ccccc3)oc2C)cc1)NCc1cccc(F)c1F
Reaction #672712
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2005_08
O=C(C=Cc1cccc(F)c1F)c1cnc2sc3c(n12)CCCCC3
Reaction #723058
3-(2,3-Difluorophenyl)-1-(6,7,8,9-tetrahydro-5H-cyclohept[d]imidazo[2,1-b]thiazol-3-yl)-2-propene-1-one
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2001_02
O=C(C=Cc1cccc(F)c1F)c1cnc2sc3c(n12)CCCCC3
Reaction #763951
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (3/10)
N#Cc1ccccc1N1CCN(C(=O)C2CC(N(Cc3ccc(F)cc3F)C(=O)OCC(Cl)(Cl)Cl)CN2Cc2cccc(F)c2F)CC1
Reaction #778667
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (3/10)
O=Cc1cc([N+](=O)[O-])cc(F)c1F
Reaction #796018
11A
Ausbeute 35.2%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2015_11
OC(c1ncc[nH]1)c1cccc(F)c1F
Reaction #821654
title compound
Ausbeute 64.6%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2009_09
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