Involved in 406 reactions

348

CCN(c1ccccc1)c1ncc(Br)c(OC)n1
Reaction #729
Yield 70.8%750 AstraZeneca ELN dataset
CCN(c1ccccc1)c1ncc(Br)c(OC)n1
Reaction #730
Yield 53.7%750 AstraZeneca ELN dataset
Nc1ccc(-c2nc(N3CC4CCC(C3)O4)cc(N3CC4CCC(C3)O4)n2)cc1
Reaction #162601
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_09
Nc1ccc(-c2cc(N3CC4CCC(C3)O4)nc(N3CC4CCC(C3)O4)n2)cc1
Reaction #162603
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_09
CCN(c1ccccc1)c1cc(C)[n+](-c2ccccc2)c(C)c1
Reaction #224607
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
CCNc1ccc(Br)cc1
Reaction #264909
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (6/10)
CCN(C(=O)NC(C)(C)c1ccc(Cl)cc1)c1ccccc1
Reaction #277669
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (6/10)
CCN(C(=O)NCc1ccc(CN(Cc2ncc(C)cc2C)C2CCCc3cccnc32)c(CO)c1)c1ccccc1
Reaction #279455
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (6/10)
CCN(C(=O)c1c(O)c2c(Cl)cccc2n(C)c1=O)c1ccccc1
Reaction #283209
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (6/10)
CCN(C(=O)c1cc([N+](=O)[O-])ccc1Br)c1ccccc1
Reaction #292421
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (6/10)
CCN(C(=O)c1c(O)c2c(Cl)cccc2n(C)c1=O)c1ccccc1
Reaction #299370
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (6/10)
CCN(C(=O)c1c(O)c2c(Cl)cccc2n(C)c1=O)c1ccccc1
Reaction #314737
crude title compound
Yield 98.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2009_07
CCN(C(=O)c1c(O)c2c(Cl)cccc2n(C)c1=O)c1ccccc1
Reaction #327395
laquinimod
Yield 98.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_02
CCN(C(=O)NCc1ccc(CN(Cc2ncc(C)cc2C)C2CCCc3cccnc32)c(CO)c1)c1ccccc1
Reaction #338263
3-(4-{[(3,5-dimethyl-pyridin-2-ylmethyl)-(5,6,7,8-tetrahydro-quinolin-8-yl)-amino]-methyl}-3-hydroxymethyl-benzyl)-1-ethyl-1-phenyl-urea
Yield 78.8%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2011_01
C=CCN(CC)c1ccccc1
Reaction #339203
allyl-ethyl-phenyl-amine
Yield 100.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2011_01
CCN(C(=O)c1c(O)c2c(OC)cccc2n(C)c1=O)c1ccccc1
Reaction #376157
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (8/10)
CCN(C(=O)c1cc(Cl)cc(OCCN(C(=O)OC(C)(C)C)c2ccncc2)c1)c1ccccc1
Reaction #400329
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (8/10)
CCN(c1ccccc1)c1ncnc2cc(Cl)ccc12.Cl
Reaction #445215
desired Compound
Yield 47.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1984_08
CCCCCC(C)N(CC)c1ccccc1
Reaction #448463
N-Ethyl-N-(1-methylhexyl)aniline
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1999_02
CCc1ccccc1NC(C)=O
Reaction #495291
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_06
Page 1Next