Involved in 332 reactions

83

Brc1ccc(N2CCC(N3CCCCC3)CC2)cc1
Reaction #748
Yield 64.4%750 AstraZeneca ELN dataset
Cc1c(N2CCC(N3CCCCC3)CC2)c(F)cn2c(=O)c(C(=O)O)cc(C3CC3)c12
Reaction #1975
title product
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
Cl.Cl.Cl.Cl.O.O=C(c1ccccc1)N1CCCC(CCCN2CCC(N3CCCCC3)CC2)(c2ccc(Cl)c(Cl)c2)C1.O=C(c1ccccc1)N1CCCC(CCCN2CCC(N3CCCCC3)CC2)(c2ccc(Cl)c(Cl)c2)C1
Reaction #78337
1-Benzoyl-3-(3,4-dichlorophenyl)-3-[3-(4-piperidinopiperid-1-yl)propyl]-piperidine Dihydrochloride Hemihydrate
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2004_03
C1CCN(C2CCNCC2)CC1
Reaction #81435
4-piperidino-piperidine
Yield 54.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1997_04
O=[N+]([O-])c1ccc(N2CCC(N3CCCCC3)CC2)cn1
Reaction #157946
2-nitro-5-[4-(1-piperidyl)-1-piperidyl]pyridine
Yield 26.7%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_09
O=[N+]([O-])c1ccc(N2CCC(N3CCCCC3)CC2)cn1
Reaction #159962
2-nitro-5-[4-(1-piperidyl)-1-piperidyl]pyridine
Yield 26.7%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_09
CS(=O)(=O)c1ccc(-c2ccc(N3CCC(N4CCCCC4)CC3)nn2)cc1
Reaction #168061
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_09
Cl
Reaction #188535
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
O=C(Nc1cc(Oc2ccc([N+](=O)[O-])cc2F)ncn1)N1CCC(N2CCCCC2)CC1
Reaction #190005
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
C1CCN(C2CCNCC2)CC1
Reaction #196497
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
Cc1ccccc1-c1nc(N2CCC(N3CCCCC3)CC2)nc2c1C(=O)N(Cc1cc(C(F)(F)F)cc(C(F)(F)F)c1)CCCN2
Reaction #208530
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
Cc1cc(CC(O)C(=O)N2CCC(N3CCCCC3)CC2)cc2cn(COCC[Si](C)(C)C)nc12
Reaction #213505
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
COc1cc2c(Nc3ccc(Oc4ccccc4)cc3)c(C#N)cnc2cc1OCCN1CCC(N2CCCCC2)CC1
Reaction #221408
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
O=C1NCc2c(Cl)nc(N3CCC(N4CCCCC4)CC3)nc2N1c1c(F)cccc1F
Reaction #222177
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
Nc1c(Cl)cc(CC(CC(=O)N2CCC(N3Cc4ccccc4NC3=O)CC2)C(=O)N2CCC(N3CCCCC3)CC2)cc1C(F)(F)F
Reaction #222585
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
CC1(C)CN(CC(NC(=O)N2CCC(N3Cc4ccccc4NC3=O)CC2)C(=O)N2CCC(N3CCCCC3)CC2)Cc2cn[nH]c21
Reaction #235820
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
CCOc1cc(C(C)(C)C)ncc1C1=NC(C)(c2ccc(Cl)cc2)C(C)(c2ccc(Cl)cc2)N1C(=O)N1CCC(N2CCCCC2)CC1
Reaction #242026
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
O=C(Nc1ccc(C(=O)N2CCC(N3CCCCC3)CC2)cc1)Nc1ccc(-c2nc(N3CCOCC3)nc(N3CCOCC3)n2)cc1
Reaction #245233
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
COc1ncc(CC(NC(=O)N2CCC(N3Cc4ccccc4NC3=O)CC2)C(=O)N2CCC(N3CCCCC3)CC2)cn1
Reaction #247154
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
Cc1cc(CC(OC(=O)N2CCC(c3cc4cccc(F)c4[nH]c3=O)CC2)C(=O)N2CCC(N3CCCCC3)CC2)cc2cn(COCC[Si](C)(C)C)nc12
Reaction #247378
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
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