4-(4-fluorobenzoyl)piperidine

O=C(c1ccc(F)cc1)C1CCN(CCO)CC1
Reaction #2553
title compound
Ausbeute 78.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
CCOC(CN1CCC(C(=O)c2ccc(F)cc2)CC1)OCC
Reaction #2556
title compound
Ausbeute 25.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
COc1cccc(C(=O)N(CCN2CCC(C(=O)c3ccc(F)cc3)CC2)c2ccccc2OC)c1
Reaction #2562
title compound
Ausbeute 46.1%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
COc1ccc(S(=O)(=O)N(CCN2CCC(C(=O)c3ccc(F)cc3)CC2)c2ccccc2OC)cc1
Reaction #2563
title compound
Ausbeute 20.7%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
O=C(c1ccc(F)cc1)C1CCN(CCCO)CC1
Reaction #54972
product
Ausbeute 48.5%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1979_04
O=C(NCCC1CC1)c1ccc(N2CCC(C(=O)c3ccc(F)cc3)CC2)nn1
Reaction #182221
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
Cn1c(=O)c2c(ncn2CCCN2CCC(C(=O)c3ccc(F)cc3)CC2)n(C)c1=O
Reaction #187878
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
Cl
Reaction #206662
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
O=C(c1ccc(F)cc1)C1CCN(CCc2ccccc2)CC1
Reaction #228231
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
O=C(c1ccc(F)cc1)C1CCN(CC2CCC3CN(c4noc5ccccc45)CCN3C2)CC1
Reaction #228247
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
O=C(c1ccc(F)cc1)C1CCN(CCCN2c3ccccc3Sc3ccc(Br)cc32)CC1
Reaction #237888
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
O=C(c1ccc(F)cc1)C1CCN(Cc2ccccc2)CC1
Reaction #238649
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
COc1ccc(S(=O)(=O)N(CCN2CCC(C(=O)c3ccc(F)cc3)CC2)c2ccccc2OC)cc1
Reaction #248598
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
O=C(c1ccc(F)cc1)C1CCN(CCCO)CC1
Reaction #254818
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
Cc1ccc2c(c1)[nH]c(=O)n2CCCN1CCC(C(=O)c2ccc(F)cc2)CC1
Reaction #256165
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
O=C(c1ccc(F)cc1)C1CCN(CCC2CCc3onc(-c4ccccc4)c3C2O)CC1
Reaction #259237
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
O=C(c1ccc(F)cc1)C1CCN(S(=O)(=O)c2ccccc2)CC1
Reaction #269545
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (6/10)
Cn1ccc2c1C(=O)CCN(CCCN1CCC(C(=O)c3ccc(F)cc3)CC1)S2(=O)=O
Reaction #272459
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (6/10)
O=C(c1ccc(F)cc1)C1CCN(CC2CSc3ccc(F)cc3C2)CC1
Reaction #272973
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (6/10)
O=C(CN1CCC(C(=O)c2ccc(F)cc2)CC1)NC1(c2ccc(=O)[nH]c2)CCCCC1
Reaction #280651
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (6/10)
Seite 1Weiter