N,N-diethylethylenediamine

N
Reaction #3541
NH3
المردود 1.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
CCN(CC)CCNC(=O)N(CCS(=O)(=O)c1ccc(OC)cc1)C(C)C
Reaction #4313
white crystalline solid
المردود 67.3%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1988_02
CCN(CC)CCNC(=S)N(CCS(=O)(=O)c1ccccc1)C(C)C
Reaction #4315
pale yellow solid
المردود 72.5%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1988_02
CCN(CC)CCNC(=O)N(CCS(=O)c1ccccc1)C(C)C
Reaction #4319
oil
المردود 55.9%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1988_02
CCN(CC)CCNC(=O)N(CCS(=O)(=O)c1ccccc1)Cc1ccccc1
Reaction #4320
oil
المردود 70.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1988_02
CCN(CC)CCNC(=O)N(C(C)C)C(C)CS(=O)(=O)c1ccccc1.O
Reaction #4323
N'-[2-(Diethylamino)ethyl]-N-(1-methylethyl)-N-[1-methyl-2-(phenylsulfonyl)ethyl]urea hydrate
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1988_02
CCN(CC)CCNC(=O)N(CCCCS(=O)(=O)c1ccccc1)C(C)C.O
Reaction #4325
clear oil
المردود 69.8%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1988_02
CCN(CC)CCNC(=O)N(CCCCCS(=O)(=O)c1ccccc1)C(C)C.O
Reaction #4326
brown oil
المردود 66.6%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1988_02
CCN(CC)CCNC(=O)c1ccc2[nH]c(-c3cc(-c4ccncc4)n[nH]c3=O)nc2c1
Reaction #40544
2-(3-Oxo-6-pyridin-4-yl-2,3-dihydropyridazin-4-yl)-1H-benzimidazole-5-carboxylic acid (2-diethylaminoethyl)amide
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
CCN(CC)CCNC(=O)COc1ccccc1
Reaction #54523
desired product
المردود 66.3%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1979_04
CCN(CC)CCNC(=NC#N)NCCCSc1nccc(NC(N)=NCC(F)(F)F)n1
Reaction #63072
4-[2-(2,2,2-trifluoroethyl)guanidino]-2-[3-(2-cyano-3-[2-diethylaminoethyl]guanidino)propylthio]pyrimidine
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1988_08
—
Reaction #64238
amide
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1995_05
CCN(CC)CCNCc1ccc(-c2ccc(C(F)(F)F)cc2)cc1
Reaction #91300
N,N-diethyl-N′-{[4′-(trifluoromethyl)-4-biphenylyl]methyl}-1,2-ethanediamine
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2016_09
CCN(CC)CCNC(=O)c1ccc(/C(=C\C2CCCC2)c2ccc(C3CC3)c(=O)[nH]2)cc1
Reaction #157778
title compound
المردود 26.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_09
CCN(CC)CCNC(=O)c1c(C)[nH]c(/C=C2\C(=O)Nc3ccc(F)cc32)c1C
Reaction #171971
Sunitinib
المردود 88.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_09
CCN(CC)CCNc1nccc(-c2sc(C3CCOCC3)nc2-c2cccc(NS(=O)(=O)c3ccoc3)c2F)n1
Reaction #174015
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
CCN(CC)CCNC(=O)c1ccc(F)cc1
Reaction #178904
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
CCN(CC)CCNC(=O)N1CCc2cc(OC)c(OC)cc2C1c1ccccc1
Reaction #182813
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
C=CCN(CCS(=O)(=O)c1ccccc1)C(=O)NCCN(CC)CC
Reaction #190750
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
CCN(CC)CCNC(=O)CN1CCCC1=O
Reaction #191129
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
الصفحة 1التالي