N',N'-diethylbutane-1,4-diamine

CCN(CC)CCCCNc1ncc2cc(-c3c(Cl)cccc3Cl)c(N)nc2n1
Reaction #3534
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
CCN(CC)CCCCNC(=O)N(CCS(=O)(=O)c1ccccc1)C(C)C
Reaction #4316
clear colorless oil
Ausbeute 26.2%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1988_02
CCN(CC)CCCCNC=C1C(=O)NC(=O)c2ccc(Br)cc21
Reaction #239754
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
CCN(CC)CCCCNC(=O)Nc1snc(OCc2c(F)cc(C)c(F)c2F)c1C(N)=O
Reaction #244190
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
CCN(CC)CCCCNc1nccc(-c2ccc(C(=O)NCCc3ccc4[nH]cc(C#N)c4c3)cc2)n1
Reaction #272237
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (6/10)
CCN(CC)CCCCNCCS(=O)(=O)c1ccccc1.O.O=C(O)C(=O)O
Reaction #417580
title compound
Ausbeute 164.4%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1990_01
CCN(CC)CCCCNc1ncc2c(n1)N(C1CCCC1)C(=O)N(c1c(F)c(OC)cc(OC)c1F)C2
Reaction #547149
title compound
Ausbeute 86.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2007_03
CCN(CC)CCCCNc1ncc2c(n1)N(C1CC1)C(=O)N(c1c(F)c(OC)cc(OC)c1F)C2
Reaction #547154
title compound
Ausbeute 83.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2007_03
CCN(CC)CCCCNc1ncc2c(n1)N(CC)C(=O)N(c1c(F)c(OC)cc(OC)c1F)C2
Reaction #547155
title compound
Ausbeute 88.4%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2007_03
CCOc1ccc(F)c(N2Cc3cnc(NCCCCN(CC)CC)nc3N(C3CCCC3)C2=O)c1F
Reaction #547173
title compound
Ausbeute 86.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2007_03
CCN(CC)CCCCNc1ncc2cc(-c3c(Cl)cccc3Cl)c(N)nc2n1
Reaction #705131
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1999_09
CCN(CC)CCCCNc1ncc2c(n1)N(C1CC1)C(=O)N(c1c(F)c(OC)cc(OC)c1F)C2
Reaction #756906
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (3/10)
CCN(CC)CCCCNC(=O)N(CCS(=O)(=O)c1ccccc1)C(C)C
Reaction #832370
clear colorless oil
Ausbeute 26.2%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1986_07
CCN(CC)CCCCNC(=O)Nc1snc(OCc2c(F)cc(C)c(F)c2F)c1C(N)=O
Reaction #837800
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2008_07
Cc1cc(F)c(COc2nsc(NC(=O)NCCCCN(C)C)c2C(N)=O)c(F)c1Cl
Reaction #837802
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2008_07
CCN(CC)CCCCNc1ncc2c(n1)N(CC)C(=O)N(c1cc(OC)cc(OC)c1)C2
Reaction #897979
DOI: 10.1039/C8SC04228DTest data from https://doi.org/10.1039/C8SC04228D
CCN(CC)CCCCNc1ncc2c(n1)N(CC)C(=O)N(c1c(F)c(OC)cc(OC)c1F)C2
Reaction #909772
DOI: 10.1039/C8SC04228DTest data from https://doi.org/10.1039/C8SC04228D
CCN(CC)CCCCNc1c2ccc(Cl)cc2nc2ccc(OC)nc12.Cl.Cl
Reaction #990324
desired product
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1980_10
CCN(CC)CCCCNC(=O)N(CCS(=O)(=O)c1ccccc1)C(C)C
Reaction #1028333
DOI: 10.1039/C8SC04228DValidation data from https://doi.org/10.1039/C8SC04228D
CCN(CC)CCCCNc1ncc2cc(-c3c(Cl)cccc3Cl)c(N)nc2n1
Reaction #1035024
DOI: 10.1039/C8SC04228DValidation data from https://doi.org/10.1039/C8SC04228D
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