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Cl.NCCC12CC3CC(CC(C3)C1)C2

CCCCCNCCC12CC3CC(CC(C3)C1)C2.Cl
Reaction #11528
titled compound
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)CCNCCC12CC3CC(CC(C3)C1)C2.Cl
Reaction #11531
titled compound
Ausbeute 23.0%DOI: 10.6084/m9.figshare.5104873.v1
NCCC12CC3CC(CC(C3)C1)C2
Reaction #11557
2-(1-adamantyl)ethylamine
DOI: 10.6084/m9.figshare.5104873.v1
CCCCCN(CCC12CC3CC(CC(C3)C1)C2)C(=O)NCCCc1ccncc1
Reaction #11558
titled compound
Ausbeute 73.6%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)OCCCc1ccncc1
Reaction #11562
titled compound
Ausbeute 97.0%DOI: 10.6084/m9.figshare.5104873.v1
Cl.O=C1CCN(CCC23CC4CC(CC(C4)C2)C3)C(=O)N1CCCc1ccncc1
Reaction #11563
titled compound
Ausbeute 79.0%DOI: 10.6084/m9.figshare.5104873.v1
CCCCCN(CCC12CC3CC(CC(C3)C1)C2)C(=S)NCCCc1ccncc1
Reaction #11564
titled compound
Ausbeute 24.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(=O)NN(CCC12CC3CC(CC(C3)C1)C2)C(=O)NCCCc1ccncc1
Reaction #11567
titled compound
Ausbeute 58.0%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)CBr
Reaction #11575
2-bromoacetic acid N-[2-(1-adamantyl)ethyl]-N-pentylamide
DOI: 10.6084/m9.figshare.5104873.v1
CCCCCN(CCC12CC3CC(CC(C3)C1)C2)C(=O)[C@H]1CCCN1.Cl
Reaction #11577
(R)-2-pyrrolidinecarboxylic acid N-[2-(1-adamantyl)ethyl]-N-pentylamide hydrochloride
DOI: 10.6084/m9.figshare.5104873.v1
CCCCCN(CCC12CC3CC(CC(C3)C1)C2)C(=O)[C@H]1CCCN1CCc1ccncc1.Cl
Reaction #11578
titled compound
Ausbeute 47.0%DOI: 10.6084/m9.figshare.5104873.v1
CCCCCN(CCC12CC3CC(CC(C3)C1)C2)C(=O)CCNC(=O)OC(C)(C)C
Reaction #11579
3-(t-butoxycarbonylamino)propionic acid N-[2-(1-adamantyl)ethyl]-N-pentylamide
Ausbeute 85.2%DOI: 10.6084/m9.figshare.5104873.v1
CCCCCN(CCC12CC3CC(CC(C3)C1)C2)C(=O)COCC(=O)OC
Reaction #11582
2-methoxycarbonylmethoxyacetic acid N-[2-(1-adamantyl)ethyl]-N-pentylamide
Ausbeute 60.0%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
CCCCCN(CCC12CC3CC(CC(C3)C1)C2)C(=S)NCCCc1ccncc1
Reaction #46682
compound
Ausbeute 24.0%DOI: 10.6084/m9.figshare.5104873.v1
CCCCCN(CCC12CC3CC(CC(C3)C1)C2)C(=O)CBr
Reaction #46687
2-bromoacetic acid N-[2-(1-adamantyl)ethyl]-N-pentylamide
DOI: 10.6084/m9.figshare.5104873.v1
CCCCCN(CCC12CC3CC(CC(C3)C1)C2)C(=O)[C@H]1CCCN1.Cl
Reaction #46689
(R)-2-pyrrolidinecarboxylic acid N-[2-(1-adamantyl)ethyl]-N-pentylamide hydrochloride
DOI: 10.6084/m9.figshare.5104873.v1
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