An 21 Reaktionen beteiligt

33939

O=C1CCc2cc(C(O)CN3CCCC(Cc4ccccc4)C3)ccc2N1
Reaction #188154
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
c1ccc(CC2CCCNC2)cc1
Reaction #217959
title compound
Ausbeute 42.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2008_06
NC(=O)c1ccc(Oc2ccc(CN3CCCC(Cc4ccccc4)C3)cc2)nc1
Reaction #217960
title compound
Ausbeute 37.4%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2008_06
COc1ccc2[nH]cc(CCCC(=O)N3CCCC(Cc4ccccc4)C3)c2c1
Reaction #296181
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (6/10)
c1ccc(CC2CCCNC2)cc1
Reaction #315417
title compound
Ausbeute 42.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2009_07
NC(=O)c1ccc(Oc2ccc(CN3CCCC(Cc4ccccc4)C3)cc2)nc1
Reaction #315418
title compound
Ausbeute 37.4%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2009_07
COC(=O)CCCCN1CCCC(Cc2ccccc2)C1
Reaction #404740
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (8/10)
c1ccc(CC2CCCNC2)cc1
Reaction #579572
title compound
Ausbeute 42.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2009_05
NC(=O)c1ccc(Oc2ccc(CN3CCCC(Cc4ccccc4)C3)cc2)nc1
Reaction #579573
title compound
Ausbeute 37.4%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2009_05
O=C(c1cccc(-c2noc(C(F)(F)F)n2)c1)N1CCCC(Cc2ccccc2)C1
Reaction #962105
(3-benzylpiperidin-1-yl)(3-(5-(trifluoromethyl)-1,2,4-oxadiazol-3-yl)phenyl)methanone
Ausbeute 44.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2015_03
NC(=O)c1ccc(Oc2ccc(CN3CCCC(Cc4ccccc4)C3)cc2)nc1
Reaction #1305802
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (5/10)
COc1ccc(CC(=O)N2CCCC(Cc3ccccc3)C2)cc1
Reaction #1308359
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (5/10)
COc1ccc(CC(=O)N2CCCC(Cc3ccccc3)C2)cc1
Reaction #1699936
3-phenylmethyl-N-(4'-methoxyphenyl)acetylpiperidine
Ausbeute 68.9%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1993_03
c1ccc(CC2CCCNC2)cc1
Reaction #1736688
3-benzylpiperidine
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1983_11
c1ccc(CC2CCCNC2)cc1
Reaction #1747757
3-benzylpiperidine
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1981_12
c1ccc(CC2CCCNC2)cc1
Reaction #1921360
3-benzylpiperidine
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1978_01
c1ccc(CC2CCCNC2)cc1
Reaction #1943065
3-benzylpiperidine
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1980_08
O=C1CCc2cc(C(O)CN3CCCC(Cc4ccccc4)C3)ccc2N1
Reaction #2027120
6-(2-(3-benzylpiperidino)-1-hydroxyethyl)-1,2,3,4-tetrahydroquinolin-2-one
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1997_12
Cl
Reaction #2212679
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (4/10)
N#Cc1ccc2[nH]cc(CCCCC3(Cc4ccccc4)CCCNC3)c2c1
Reaction #2230655
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (4/10)
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