N,N,N'-triethylethylenediamine

CCN(CC)CCN(CC)C(=O)NCCS(=O)(=O)c1ccccc1.O=C(O)CC(O)(CC(=O)O)C(=O)O
Reaction #4312
white crystalline solid
المردود 52.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1988_02
CCN(CC)CCN(CC)C(=O)c1ccccc1Nc1ccnc2c(C(F)(F)F)cccc12
Reaction #256064
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
CCN(CC)CCN(CC)C(=O)Cc1ccc(Nc2ccnc3cc(Cl)ccc23)cc1.Cl.Cl
Reaction #312311
2-[4-(7-chloro-4-quinolylamino)phenyl]-N-(2-diethylaminoethyl)-N-ethyl acetamide dihydrochloride
المردود 177.8%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1980_11
CCN(CC)CCN(CC)C(=O)CO[C@@H]1C[C@H](C)CC[C@H]1C(C)C
Reaction #336026
N-(2- diethylaminoethyl)-N-(ethyl)-((1R,3R,4S)-1-methyl-4-isopropylcyclohex-3-yloxy)acetamide
المردود 60.4%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1993_05
CCN(CC)CCN(CC)C(=O)N1CCC(Oc2cc(Cl)cc(Cl)c2)C1
Reaction #551616
dark oil
المردود 78.7%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1985_10
CCN(CC)CCN(CC)C(=O)NCCS(=O)(=O)c1ccccc1.O=C(O)CC(O)(CC(=O)O)C(=O)O
Reaction #832366
white crystalline solid
المردود 52.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1986_07
CCCCCCC/C=C/C(=O)N(CC)CCN(CC)CC
Reaction #966084
aimed compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2015_03
CCN(CC)CCN(CC)C(=O)c1ccc(Nc2ccnc3c(C(F)(F)F)cccc23)cc1
Reaction #1020244
DOI: 10.1039/C8SC04228DValidation data from https://doi.org/10.1039/C8SC04228D
CCN(CC)CCN(CC)C(=O)N1CCC(Oc2cc(Cl)cc(Cl)c2)C1
Reaction #1030361
DOI: 10.1039/C8SC04228DValidation data from https://doi.org/10.1039/C8SC04228D
CC(C)(C)OC(=O)CC(CCCOCc1ccccc1)C(=O)N1C(=O)OCC1Cc1ccccc1
Reaction #1045980
DOI: 10.1039/C8SC04228DValidation data from https://doi.org/10.1039/C8SC04228D
CCN(C=C1C(=O)OC(COC)C2(C)C1=C(O)C(=O)C1=C2C(OC(C)=O)CC2(C)C(O)CCC12)CCN(CC)CC
Reaction #1533195
product
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_02
CCN(CC)CCN(CC)C(=O)NCCS(=O)(=O)c1ccccc1
Reaction #1623452
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (1/10)
CCN(CC)CCN(CC)C(=O)COC1CC(C)CCC1C(C)C
Reaction #1623651
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (1/10)
CC(C)(C)OC(=O)CC(CCCOCc1ccccc1)C(=O)N1C(=O)OC[C@H]1Cc1ccccc1
Reaction #1999254
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_12
Cc1nn(C)c2c1N(C(=O)CN1CCCN(C)CC1)c1ccccc1NC2=O
Reaction #2145781
4-[(hexahydro-4-methyl-1H-1,4-diazepin-1-yl)acetyl]-1,3-dimethyl-1,4,9,10-tetrahydropyrazolo[4,3-b][1,5]benzodiazepin-10-one
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1982_03
CCN(CC)CCN(CC)C(=O)c1ccccc1Nc1ccnc2c(C(F)(F)F)cccc12
Reaction #2285667
title compound
المردود 46.2%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1982_11
CCN(CC)CCN(CC)C(=O)c1ccc(Nc2ccnc3c(C(F)(F)F)cccc23)cc1
Reaction #2285670
N-(2-diethylaminoethyl)-N-ethyl-4-(8-trifluoromethyl-4-quinolylamino)benzamide
المردود 64.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1982_11