N',N'-bis(2-aminoethyl)ethane-1,2-diamine

CNC(Cc1ccccc1)C(=O)NN(C)C(=O)OC(C)(C)C
Reaction #185237
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
COC(=O)CCN(CCC(=O)OC)CCN(CCN(CCC(=O)OC)CCC(=O)OC)CCN(CCC(=O)OC)CCC(=O)OC
Reaction #320603
Tris-[N,N-bis-(methoxycarbonylethyl)-2-aminoethyl]-amine
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1997_01
CCOC(=O)NCCN(CCNC(=O)OCC)CCNC(=O)OCC
Reaction #344329
tris(2-carbethoxyaminoethyl)amine
Ausbeute 85.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1993_11
CC(C)(C)OC(=O)COc1cccc(CN(Cc2ccc(-n3cccn3)cc2)S(=O)(=O)c2ccc(Cl)cc2)c1
Reaction #369437
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (8/10)
NCCN(CCN)CCNC1CCCCCCCCCCCCCC1
Reaction #415102
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1993_12
CC(=NO)C(C)(C)NCCN(CCN)CCNC(C)(C)C(C)=NO
Reaction #567848
Compound 15
Ausbeute 9.5%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2003_11
—
Reaction #700398
crude product
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1999_12
NS(=O)(=O)NCCNc1nonc1C(=NO)Nc1ccc(F)c(Br)c1
Reaction #719727
crude desired product
Ausbeute 90.3%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2016_04
C=CC(N)=O.NCCN(CCN)CCN
Reaction #738722
TAEA acrylamide
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2001_08
NCCN=Cc1ccc[nH]1
Reaction #942655
[(((pyrrole-2-yl)methylidene)amino)ethyl]amine
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2007_08
C=CCOC(=O)[C@H](Cc1ccc(OC(C)(C)C)cc1)NC(=O)[C@@H](N)COC(C)(C)C
Reaction #994633
crude product
Ausbeute 88.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2011_09
CC(C)(C)OC(=O)COc1cccc(CN(Cc2ccc(-n3cccn3)cc2)S(=O)(=O)c2ccc(-c3ccccn3)s2)c1
Reaction #1025345
DOI: 10.1039/C8SC04228DValidation data from https://doi.org/10.1039/C8SC04228D
O=C(OCCN1CCOCC1)c1ccc(I)cc1
Reaction #1129222
2-morpholinoethyl 4-iodobenzoate
Ausbeute 73.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_10
NCCN=Cc1ccc[nH]1
Reaction #1269191
[(((pyrrole-2-yl)methylidene)amino)ethyl]amine
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2007_10
NCCN(CCN)CCNC1CCCCCCCCCCCCCC1
Reaction #1291105
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (5/10)
CC(C)(C)OC(=O)COc1cccc(CN(Cc2ccc(-n3cccn3)cc2)C(=O)N2CCCC2)c1
Reaction #1326146
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (5/10)
NCCN(CCN)CCN
Reaction #1504637
tris(2-aminoethyl)amine
Ausbeute 45.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1999_03
NCCN(CCN)CCNC1CCCCCCCCCCCCCC1
Reaction #1579513
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1994_12
O=C(OCCN1CCOCC1)c1ccc(I)cc1
Reaction #1627537
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (1/10)
COC(=O)C(Cc1ccc(Cl)c(Cl)c1)NC(=O)c1ccc(I)cc1NS(=O)(=O)c1cccc2nsnc12
Reaction #1631891
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (1/10)
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