#894046

Cl.O=C1COc2cc(Cl)c(CNC3CCN(C[C@@H]4Cn5c(=O)ccc6ncc(F)c4c65)CC3)nc2N1
Reaction #43636
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
CN(CC1CN(C2CCCCCC2)C(=O)C1(C)C)c1ccccc1F
Reaction #44487
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
CN(Cc1ccc(C(=O)O)cc1)CC1CCCCN1Cc1ccc(Oc2ccc(Br)cc2)cc1
Reaction #44803
4-[[[[(RS)-1-[[4-(4-bromophenoxy)phenyl]methyl]-2-piperidinyl]methyl]methylamino]methyl]benzoic acid
Ausbeute 13.2%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
CN(C)C1CCNCC1.Cl.Cl
Reaction #51231
4-(dimethylamino)piperidine.dihydrochloride
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2005_02
CN(CCCc1ccc(F)cc1)C1CCC(c2ccc3[nH]c(=O)sc3c2)CC1
Reaction #173046
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
CCc1nc2ccccc2n1-c1nc(N2CCOCC2)c2nc(CN3CC(N4CCNC(=O)C4)C3)n(C)c2n1
Reaction #173197
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
CCCCN1CCN(c2ccccc2C2=CCCCCCC2)CC1
Reaction #173226
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
CCOC(=O)c1ccc(N2CC(C)N(C)C(C)C2)cc1
Reaction #173519
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
OC1CCCN(Cc2ccccc2)C1
Reaction #173556
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
CC(C)(C)OC(=O)N1CCC(CN2CCCCC2)CC1
Reaction #173657
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
CC(C)(C)OC(=O)N1CCCC1CNCc1cc2ccccc2cn1
Reaction #173671
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
CN(c1cc(OC(F)(F)F)cc2cc(C(=O)NCC(CN3CCOCC3)SCc3ccccc3)[nH]c12)S(=O)(=O)c1cccs1
Reaction #173877
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
CCN1Cc2cc(NCc3ccc(Cl)cc3)ccc2C1=O
Reaction #174026
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
COCCNCc1nc(NCC(c2ccccc2)c2ccccc2)c2ncn(C3OC(COC)C(O)C3O)c2n1
Reaction #175043
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
CC(C)CCNCc1cc(F)c(Oc2ccc3c(c2)OC(C)(C)OC3=O)c(F)c1
Reaction #175052
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
Cl
Reaction #175057
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
COc1ccc(CN(Cc2ccc(OC)cc2)c2ncc(-c3nc(N4CCOCC4)nc4c3CCN4c3ccc(CN4CCN(C)CC4)cc3)cn2)cc1
Reaction #175158
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
CCCCOc1nc(N)c2[nH]c(=O)n(CCCN(CCCN3CCOCC3)Cc3ccccc3)c2n1
Reaction #175176
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
COc1cc(-c2ccncc2)c2ncc(=O)n(CCN3CCC(NCc4cc5c(cn4)OCCO5)CC3)c2c1
Reaction #175253
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
COC(CCCCCCN1CCC(C(C(N)=O)(c2ccccc2)c2ccccc2)C1)OC
Reaction #175355
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
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