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CCCCCN(CCC12CC3CC(CC(C3)C1)C2)C(=O)NCCCc1ccncc1
Reaction #11558
titled compound
Ausbeute 73.6%DOI: 10.6084/m9.figshare.5104873.v1
CCCN(CCC12CC3CC(CC(C3)C1)C2)C(=O)CCCCc1ccncc1
Reaction #11559
titled compound
Ausbeute 33.0%DOI: 10.6084/m9.figshare.5104873.v1
CNCCN(CCC12CC3CC(CC(C3)C1)C2)C(=O)NCCCc1ccncc1.Cl.Cl
Reaction #11560
titled compound
DOI: 10.6084/m9.figshare.5104873.v1
CCCCCN(CCC12CC3CC(CC(C3)C1)C2)C(=O)NCCCc1cc[n+](C)cc1.[I-]
Reaction #11561
titled compound
Ausbeute 96.0%DOI: 10.6084/m9.figshare.5104873.v1
CCCCCN(CCC12CC3CC(CC(C3)C1)C2)C(=O)OCCCc1ccncc1
Reaction #11562
titled compound
Ausbeute 97.0%DOI: 10.6084/m9.figshare.5104873.v1
CN(CCCc1ccncc1)C(=O)N(C)CCC12CC3CC(CC(C3)C1)C2
Reaction #11568
titled compound
Ausbeute 141.6%DOI: 10.6084/m9.figshare.5104873.v1
CCCCCN(CCC12CC3CC(CC(C3)C1)C2)C(=O)NCCCc1ccncc1.Cl
Reaction #11570
titled compound
Ausbeute 43.0%DOI: 10.6084/m9.figshare.5104873.v1
CCCCCN(CCC12CC3CC(CC(C3)C1)C2)C(=O)NCCCc1cc[n+]([O-])cc1
Reaction #11573
titled compound
Ausbeute 94.2%DOI: 10.6084/m9.figshare.5104873.v1
COCCN(C)CCN(CCC12CC3CC(CC(C3)C1)C2)C(=O)NCCCc1ccncc1
Reaction #11574
titled compound
Ausbeute 32.1%DOI: 10.6084/m9.figshare.5104873.v1
CCCCCN(CCC12CC3CC(CC(C3)C1)C2)C(=O)CNCCc1ccncc1
Reaction #11576
titled compound
Ausbeute 41.6%DOI: 10.6084/m9.figshare.5104873.v1
CCCCCN(CCC12CC3CC(CC(C3)C1)C2)C(=O)CCNCc1ccncc1
Reaction #11580
titled compound
Ausbeute 36.1%DOI: 10.6084/m9.figshare.5104873.v1
NCCN(CCC12CC3CC(CC(C3)C1)C2)C(=O)NCCCc1ccncc1
Reaction #11581
titled compound
Ausbeute 21.7%DOI: 10.6084/m9.figshare.5104873.v1
CCCN(CCC12CC3CC(CC(C3)C1)C2)C(=O)CCCCc1ccncc1
Reaction #46679
compound
Ausbeute 33.0%DOI: 10.6084/m9.figshare.5104873.v1
CNCCN(CCC12CC3CC(CC(C3)C1)C2)C(=O)NCCCc1ccncc1.Cl.Cl
Reaction #46680
1-[2-(1-Adamantyl)ethyl]-1-(2-methylaminoethyl)-3-[3-(4-pyridyl)propyl]urea dihydrochloride
DOI: 10.6084/m9.figshare.5104873.v1
CCCCCN(CCC12CC3CC(CC(C3)C1)C2)C(=O)OCCCc1ccncc1
Reaction #46681
compound
Ausbeute 97.0%DOI: 10.6084/m9.figshare.5104873.v1
CN(CCCc1ccncc1)C(=O)N(C)CCC12CC3CC(CC(C3)C1)C2
Reaction #46684
compound
Ausbeute 141.6%DOI: 10.6084/m9.figshare.5104873.v1
COCCN(C)CCN(CCC12CC3CC(CC(C3)C1)C2)C(=O)NCCCc1ccncc1
Reaction #46686
compound
Ausbeute 32.1%DOI: 10.6084/m9.figshare.5104873.v1
CCCCCN(CCC12CC3CC(CC(C3)C1)C2)C(=O)CNCCc1ccncc1
Reaction #46688
compound
Ausbeute 41.6%DOI: 10.6084/m9.figshare.5104873.v1
CCCCCN(CCC12CC3CC(CC(C3)C1)C2)C(=O)CCNCc1ccncc1
Reaction #46691
compound
Ausbeute 36.0%DOI: 10.6084/m9.figshare.5104873.v1
NCCN(CCC12CC3CC(CC(C3)C1)C2)C(=O)NCCCc1ccncc1
Reaction #46692
compound
Ausbeute 21.7%DOI: 10.6084/m9.figshare.5104873.v1
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