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557868

Cl.O=C(CCl)NC1CN2CCC1CC2
Reaction #5597
solid
Ausbeute 144.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)c1cc(SCC(=O)NC2CN3CCC2CC3)cc(C(C)(C)C)c1O.Cl
Reaction #5598
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CNC1CN(Cc2ccccc2)CCC1C
Reaction #7307
(1-Benzyl-4-methyl-piperidin-3-yl)-methyl-amine
Ausbeute 90.0%DOI: 10.6084/m9.figshare.5104873.v1
CN[C@@H]1CN(Cc2ccccc2)CC[C@@H]1C.Cl
Reaction #7308
Cis-(1-Benzyl-4-methyl-piperidin-3-yl)-methyl-amine hydrochloride salt
Ausbeute 37.5%DOI: 10.6084/m9.figshare.5104873.v1
CNC1CN(Cc2ccccc2)CCC1C
Reaction #8797
title compound
Ausbeute 69.0%DOI: 10.6084/m9.figshare.5104873.v1
CC1CCN(Cc2ccccc2)CC1N(C)c1ncnc2[nH]ccc12
Reaction #8798
title compound
Ausbeute 50.0%DOI: 10.6084/m9.figshare.5104873.v1
—
Reaction #57337
two
Ausbeute 79.0%DOI: 10.6084/m9.figshare.5104873.v1
CNC1C2CCN(CC2)C1Cc1cccnc1
Reaction #59356
3-(methylamino)-2-((3-pyridinyl)methyl)-1-azabicyclo[2.2.2]octane
DOI: 10.6084/m9.figshare.5104873.v1
CNC1CN(Cc2ccccc2)CCC1C
Reaction #72690
title compound
Ausbeute 69.0%DOI: 10.6084/m9.figshare.5104873.v1
CC1CCN(Cc2ccccc2)CC1N(C)c1ncnc2[nH]ccc12
Reaction #72691
title compound
Ausbeute 50.0%DOI: 10.6084/m9.figshare.5104873.v1
CNC1C2CCN(CC2)C1Cc1cccnc1
Reaction #72938
3-(methylamino)-2-((3-pyridinyl)methyl)-1-azabicyclo[2.2.2]octane
DOI: 10.6084/m9.figshare.5104873.v1
CNC1CCC(CNC(=O)c2cccc3cccnc23)N(C(=O)c2ccccc2-c2ccccc2)C1
Reaction #89102
N-((1-(Biphenylcarbonyl)-5-(methylamino)piperidin-2-yl)methyl)quinoline-8-carboxamide
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)N[C@@H]1CCCN(CC(=O)O)C1=O
Reaction #158925
(R)-(3-tert-butoxycarbonylamino-2-oxo-piperidin-1-yl)-acetic acid
Ausbeute 95.1%DOI: 10.6084/m9.figshare.5104873.v1
Cc1ccc(CN2CC3(Nc4ccc5[nH]ncc5c4)CCC2CC3)cc1
Reaction #162884
title compound
DOI: 10.6084/m9.figshare.5104873.v1
COc1cccc(CN2CC3(Nc4ccc5[nH]ncc5c4)CCC2CC3)c1
Reaction #162886
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)N[C@@H]1CCCN(CC(=O)O)C1=O
Reaction #166879
(R)-(3-tert-butoxycarbonylamino-2-oxo-piperidin-1-yl)-acetic acid
Ausbeute 95.1%DOI: 10.6084/m9.figshare.5104873.v1
Cc1noc(C)c1-c1cncc(N2CC3CC4CC2CN(C4)C3)c1
Reaction #167606
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)CN1CCCC(NC(=O)c2ccc(OCc3c(-c4ccccc4)noc3C)nc2)C1
Reaction #170329
title compound
Ausbeute 81.2%DOI: 10.6084/m9.figshare.5104873.v1
Cc1onc(-c2ccccc2)c1COc1ccc(C(=O)NC2CCCN(CC(=O)O)C2)cn1
Reaction #170330
title compound
Ausbeute 84.8%DOI: 10.6084/m9.figshare.5104873.v1
Cc1onc(-c2cccc(F)c2)c1COc1ccc(C(=O)O)cn1
Reaction #170389
title compound
Ausbeute 95.0%DOI: 10.6084/m9.figshare.5104873.v1
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