2-(N-Ethylanilino)ethanol

CCN(CCOC(C)=O)c1ccccc1
Reaction #7434
2-(ethylphenylamino)ethyl acetate
收率 99.9%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
CCN(CCOCc1ccc(C(=O)c2ccccc2)cc1)c1ccccc1
Reaction #75451
desired product
收率 80.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2004_03
CCNCCOC(=O)c1ccccc1
Reaction #336231
product
收率 96.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1993_05
CCN(CCOC(C)=O)c1ccccc1
Reaction #363925
2-(N-ethylanilino)ethyl acetate
收率 99.9%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2002_03
CCN(CCOCc1ccc(C(=O)c2ccccc2)cc1)c1ccccc1
Reaction #390488
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (8/10)
CCN(CCOCOC)c1ccccc1
Reaction #443409
N-ethyl-N-[2-(methoxymethyl)oxyethyl]aniline
收率 89.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_11
C=CC(=O)OCCN(CC)c1ccccc1
Reaction #606439
N-(2-acryloyloxyethyl)-N-ethylaniline
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2015_08
CCN(CCOS(=O)(=O)O)c1ccccc1
Reaction #624812
2-[ethyl(phenyl)amino]ethyl hydrogen sulfate
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_10
CCN(CCO)c1ccc(C2=CC(=O)C(=O)c3ccccc32)cc1
Reaction #624815
4-(4-(ethyl(2-hydroxyethyl)amino)phenyl)naphthalene-1,2-dione
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_10
CCN(CCOCc1ccc(C(=O)c2ccccc2)cc1)c1ccccc1
Reaction #635023
desired product ( XIV )
收率 80.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2011_05
CCN(CCN=[N+]=[N-])c1ccccc1
Reaction #684310
N-ethyl-N-β-azido-ethylaniline
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1977_03
CCN(CCO)c1ccc(N=O)cc1
Reaction #740322
N-Ethyl-N-2-hydroxyethyl-p-nitrosoaniline
收率 59.6%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1987_06
CCCOCCN(CC)c1ccccc1
Reaction #1035272
DOI: 10.1039/C8SC04228DValidation data from https://doi.org/10.1039/C8SC04228D
CCN(CCOC(C)=O)c1ccccc1
Reaction #1070755
2-(N-ethyl-N-phenylamino)ethylethanoate
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2005_03
CCN(CCO)c1ccc(/N=N/c2nc(Cl)c(C=O)s2)cc1
Reaction #1099222
4-chloro-2-((E)-{4-[ethyl(2-hydroxyethyl)amino]phenyl}-diazenyl)-1,3-thiazole-5-carbaldehyde
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2011_07
CCN(CCCl)c1ccccc1
Reaction #1140740
intermediate 3a
收率 50.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2016_07
CCN(CCCl)c1ccccc1
Reaction #1140767
intermediate 15a
收率 50.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2016_07
CCN(CCO)c1ccc(N=Nc2nc(Cl)c(C=O)s2)cc1
Reaction #1646494
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (1/10)
CCN(CCO)c1ccc(/N=N/c2nc(Cl)c(C=O)s2)cc1
Reaction #1776741
4-chloro-2-((E)-{4-[ethyl(2-hydroxyethyl)amino]phenyl}-diazenyl)-1,3-thiazole-5-carbaldehyde
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2012_04
CCN(CCOCc1ccc(C(=O)c2ccccc2)cc1)c1ccccc1
Reaction #1884458
desired product
收率 80.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_04
第 1 页下一页