Impliqué dans 133 réactions

588358

COC(=O)N(Cc1cc(C(F)(F)F)cc(C(F)(F)F)c1)Cc1cc(C(F)(F)F)ccc1-c1cc(-c2nc(C)no2)ccc1OC
Reaction #45370
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
Cc1noc([C@@H](N)C(C)C)n1
Reaction #52039
(S)-5-(1-amino-2-methylpropyl)-3-methyl-1,2,4-oxadiazole
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2005_02
COc1ccc(N)c(-c2nc(C)no2)c1
Reaction #81522
title compound
Rendement 72.4%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1997_04
CCc1csc([C@H](Cc2ccc([N+](=O)[O-])cc2)NC(=O)C(Cc2ccccc2)c2nc(C)no2)n1
Reaction #88318
desired product
Rendement 94.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2016_09
Cc1noc(C2CN(Cc3ccccc3)CC3(CCN(C(=O)c4ccc(OC(C)C)c(C)c4)CC3)O2)n1
Reaction #160220
[8-benzyl-10-(3-methyl-1,2,4-oxadiazol-5-yl)-11-oxa-3,8-diazaspiro[5.5]undecan-3-yl]-(4-isopropoxy-3-methyl-phenyl)methanone
Rendement 39.1%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_09
COc1cc(C(=O)ON=C(C)N)cc([N+](=O)[O-])c1OC
Reaction #210163
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
COc1ccc(CCNc2cc(-c3cccc(C(=O)NC(C)=N)c3)nc(OC)n2)cc1
Reaction #303326
N-(1-imino-ethyl)-3-{2-methoxy-6-[2-(4-methoxy-phenyl)-ethylamino]-pyrimidin-4-yl}-benzamide
Rendement 69.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2012_06
CON=C1C[C@@H](Cc2nc(C)no2)N(C(=O)c2ccc(-c3ccccc3)cc2)C1
Reaction #313153
(3EZ,5S)-1-(biphenyl-4-ylcarbonyl)-5-[(3-methyl-1,2,4oxadiazol-5-yl)methyl]pyrrolidin-3-one O-methyloxime
Rendement 102.4%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2009_07
COc1cc(I)ccc1-c1nc(C)no1
Reaction #359882
desired product
Rendement 39.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2008_11
COc1cc(C(=O)ON=C(C)N)cc([N+](=O)[O-])c1OC
Reaction #361729
N'-[(3,4-dimethoxy-5-nitrobenzoyl)oxy]acetamidine
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1995_02
CC(N)=NOC(=O)C(NC(=O)c1nc(-c2ccccc2)n2c1CN(C(=O)OC(C)(C)C)CC2)C(C)(C)C
Reaction #381762
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (8/10)
COc1cc(C(=O)ON=C(C)N)cc([N+](=O)[O-])c1OC
Reaction #391223
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (8/10)
CCc1csc([C@H](Cc2ccc([N+](=O)[O-])cc2)NC(=O)C(Cc2ccccc2)c2nc(C)no2)n1
Reaction #422204
desired product
Rendement 94.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_11
CCCc1c2nc(-c3cc(-c4nc(C)no4)cnc3OCC(C)C)[nH]c(=O)c2nn1C
Reaction #441370
product
Rendement 39.4%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2004_06
CC(N)=NOC(=O)[C@@H]1CCCCN1S(=O)(=O)c1ccc(F)cc1
Reaction #484873
N′1-[((2S)-1-[(4-fluorophenyl)sulfonyl]-2-piperidylcarbonyl)oxy]ethanimidamide
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2003_08
Cc1noc(-c2cncc(C(=O)O)c2)n1
Reaction #486982
5-(3-methyl-1,2,4-oxadiazol-5-yl)-3-pyridinecarboxylic acid
Rendement 32.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_10
C/C(N)=N/OC(=O)c1cc2nccc(Cl)c2s1
Reaction #503083
title compound
Rendement 46.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2012_01
CCc1csc([C@H](Cc2ccc([N+](=O)[O-])cc2)NC(=O)C(Cc2ccccc2)c2nc(C)no2)n1
Reaction #512062
desired product
Rendement 94.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2012_01
—
Reaction #538619
gum
Rendement 61.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_07
Cc1noc(C=Cc2ccccc2O)n1
Reaction #547779
title compound
Rendement 58.4%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2007_03
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