4-ethynylaniline

C#Cc1ccc(NC(=O)CCCC(=O)O)cc1
Reaction #47737
yellow white product 24
Ausbeute 96.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
CCOC(=O)c1c(C)nc(C#Cc2ccc(N)cc2)n1C
Reaction #77232
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2004_03
Nc1ccc(C#Cc2ccc(OC(F)(F)F)cc2)cc1
Reaction #181626
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
CC(C)(C)c1cc2ncc(C#Cc3ccc(N)cc3)cn2n1
Reaction #190946
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
C#Cc1ccc(NC(=O)C(Cl)Cl)cc1
Reaction #192203
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
COC(=O)CCCCS(=O)(CCCCC(=O)OC)=NC(=O)c1cnc(N)c(C#Cc2ccc(N)cc2)c1
Reaction #200859
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
CCOC(=O)c1c(C)nc(C#Cc2ccc(N)cc2)n1C
Reaction #285427
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (6/10)
C#Cc1ccc(N=C=O)cc1
Reaction #289304
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (6/10)
C#Cc1ccc(NC(=O)C23CCC(NCC(=O)N4C[C@@H](F)C[C@H]4C#N)(CC2)CC3)cc1
Reaction #315208
(2S,4S)-1-[[N-[4-[N-(4-ethynylphenyl)amino]carbonylbicyclo[2.2.2]oct-1-yl]amino]acetyl]-4-fluoropyrrolidine-2-carbonitrile
Ausbeute 15.3%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2009_07
C#Cc1ccc(NS(C)(=O)=O)cc1
Reaction #405532
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (8/10)
C#Cc1ccc(NC(C)=O)cc1
Reaction #427507
N-(4-ethynylphenyl)acetamide
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_11
Nc1ccc(C#Cc2ccc(I)cc2)cc1
Reaction #434790
desired product
Ausbeute 354.1%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2007_02
CC(=O)Nc1ccccc1C#Cc1ccc(N)cc1
Reaction #538438
N-[2-(4-Amino-phenylethynyl)-phenyl]-acetamide
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_07
Nc1ccc(C#Cc2ccc(OC(F)(F)F)cc2)cc1
Reaction #538457
4-(4-Trifluoromethoxy-phenylethynyl)-phenylamine
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_07
CCOC(=O)c1c(C)nc(C#Cc2ccc(N)cc2)n1C
Reaction #575657
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2005_12
Nc1ccc(C#Cc2ccc(I)cc2)cc1
Reaction #577203
desired product
Ausbeute 354.1%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2009_05
C#Cc1ccc(NS(C)(=O)=O)cc1
Reaction #595515
title compound
Ausbeute 80.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2015_08
C#Cc1ccc(NC(=O)c2cnn3c(C)cc(C)nc23)cc1
Reaction #618145
N-(4-ethynylphenyl)-5,7-dimethylpyrazolo[1,5-a]pyrimidine-3-carboxamide
Ausbeute 46.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2016_05
CCOC(=O)c1c(C)nc(C#Cc2ccc(N)cc2)n1C
Reaction #671884
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2005_08
C#Cc1ccc(NC(=O)Nc2cccc(C)c2)cc1
Reaction #677077
1-(4-ethynylphenyl)-3-(3-methylphenyl)urea
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2016_01
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