1-(4-pyridyl)piperazine

COC(=O)COc1ccc(C(=O)CN2CCN(c3ccncc3)CC2)cc1
Reaction #2296
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
COC(=O)Cc1ccc(C(=O)CN2CCN(c3ccncc3)CC2)cc1
Reaction #2300
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
COC(=O)COc1ccc(C(=O)C(C)N2CCN(c3ccncc3)CC2)cc1
Reaction #2301
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
COC(=O)C(C)(C)Oc1ccc(C(=O)CN2CCN(c3ccncc3)CC2)cc1
Reaction #2313
methyl 2-[4-[2-[4-(4-pyridyl)piperazin-1-yl]acetyl]phenoxy]isobutyrate
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
CCOC(=O)COc1ccc(C(=O)CN2CCN(c3ccncc3)CC2)cc1
Reaction #2314
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
CC(C)OC(=O)COc1ccc(C(=O)CN2CCN(c3ccncc3)CC2)cc1
Reaction #2315
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
COC(=O)COc1ccc(C(=O)C(C)(C)N2CCN(c3ccncc3)CC2)cc1
Reaction #2328
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
COC(=O)COc1ccc(C(=O)C(C)CN2CCN(c3ccncc3)CC2)cc1
Reaction #2330
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
COC(=O)CCCc1ccc(CN2CCN(c3ccncc3)CC2)cc1
Reaction #2331
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
CC(C)(C)OC(=O)n1c(-c2ccc(Cl)c3c2C(=O)NC3)cc2cc(CN3CCN(c4ccncc4)CC3)ccc21
Reaction #49337
4-chloro-7-(1-(tert-butoxycarbonyl)-5-[4-(pyridin-4-yl)piperazin-1-ylmethyl]indol-2-yl)isoindolinone
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
N#CC1(N2CCN(c3ccncc3)CC2)CCN(Cc2ccccc2)CC1
Reaction #74280
1-Benzyl-4-(4-(pyridin-4-yl)piperazin-1-yl)piperidine-4-carbonitrile
Ausbeute 47.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_09
COc1nn(-c2ccccc2)c2cc(N3CCN(c4ccncc4)CC3)ccc12.Cl
Reaction #155893
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_09
NS(=O)(=O)N1CCN(c2ccncc2)CC1
Reaction #177235
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
CCn1cc(C(=O)O)c(=O)c2ccc(N3CCN(c4ccncc4)CC3)cc21
Reaction #193963
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
CCn1cc(C(=O)O)c(=O)c2cc(F)c(N3CCN(c4ccncc4)CC3)cc21
Reaction #194654
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
COc1ccc(C(=O)N2CCN(c3ccncc3)CC2)cc1OCCc1ccc(Cl)cc1Cl
Reaction #195184
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
O=C(COCC1CCCCN1S(=O)(=O)c1ccc(Br)cc1)N1CCN(c2ccncc2)CC1
Reaction #242391
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
O=C(c1ccc(S(=O)(=O)c2ccc3cc(Cl)ccc3c2)cc1)N1CCN(c2ccncc2)CC1
Reaction #247220
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
COC(=O)COc1ccc(C(=O)C(C)N2CCN(c3ccncc3)CC2)cc1
Reaction #248694
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
COC(=O)c1ccc(CN2CCN(c3ccncc3)CC2)cc1
Reaction #248980
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
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