An 26 Reaktionen beteiligt

19476

NC(=O)[C@H]1CCCC[C@H]1N(Cc1ccc(F)c(Cl)c1)S(=O)(=O)c1ccc(Cl)cc1
Reaction #7129
titled compound
Ausbeute 43.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
O=C1CCCCN1Cc1ccc(F)c(Cl)c1
Reaction #46261
title product
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
Fc1ccc(CBr)cc1Cl
Reaction #201131
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
O=C1CCCCN1Cc1ccc(F)c(Cl)c1
Reaction #240667
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
O=C1CCCCN1Cc1ccc(F)c(Cl)c1
Reaction #397572
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (8/10)
CCN1C[C@H](C)n2c(c(OC)c3c(=O)n(Cc4ccc(F)c(Cl)c4)nc(C(=O)NC)c32)C1=O
Reaction #581301
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2009_05
CCN1C[C@H](C)n2c(c(OC)c3c(=O)n(Cc4ccc(F)c(Cl)c4)nc(N)c32)C1=O
Reaction #581320
title material
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2009_05
Fc1ccc(CBr)cc1Cl
Reaction #670102
expected product
Ausbeute 97.9%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1999_07
CCN1CC(C)n2c(c(OC)c3c(=O)n(Cc4ccc(F)c(Cl)c4)nc(C(=O)NC)c32)C1=O
Reaction #767342
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (3/10)
NC(=O)C1CCCCC1N(Cc1ccc(F)c(Cl)c1)S(=O)(=O)c1ccc(Cl)cc1
Reaction #784426
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (3/10)
O=C1CCCCN1Cc1ccc(F)c(Cl)c1
Reaction #886431
DOI: 10.1039/C8SC04228DTest data from https://doi.org/10.1039/C8SC04228D
CCN1CC(C)n2c(c(OC)c3c(=O)n(Cc4ccc(F)c(Cl)c4)nc(N)c32)C1=O
Reaction #898449
DOI: 10.1039/C8SC04228DTest data from https://doi.org/10.1039/C8SC04228D
O=C1C(=O)c2ccccc2C2=C1SCC1(CCN(Cc3ccc(F)c(Cl)c3)CC1)O2
Reaction #1038461
DOI: 10.1039/C8SC04228DValidation data from https://doi.org/10.1039/C8SC04228D
CCN1CC(C)n2c(c(OC)c3c(=O)n(Cc4ccc(F)c(Cl)c4)cc(C(=O)OC)c32)C1=O
Reaction #1238791
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (7/10)
CN(C)C(=O)c1c2c(c(O)c(=O)n1C)C(=O)N(Cc1ccc(F)c(Cl)c1)CC2
Reaction #1651651
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (1/10)
O=C1C(=O)c2ccccc2C2=C1SCC1(CCN(Cc3ccc(F)c(Cl)c3)CC1)O2
Reaction #1752522
Compound 142
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2011_10
CN(C)C(=O)c1c2c(c(OCc3ccc(F)c(Cl)c3)c(=O)n1C)C(=O)N(Cc1ccc(F)c(Cl)c1)CC2
Reaction #1904505
6-(3-chloro-4-fluorobenzyl)4-[(3-chloro-4-fluorobenzyl)oxy]-N,N,2-trimethyl-3,5-dioxo-2,3,5,6,7,8-hexahydro-2,6-naphthyridine-1-carboxamide
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2009_10
O=C1CCCCN1Cc1ccc(F)c(Cl)c1
Reaction #1904506
1-(3-Chloro-4-fluorobenzyl)piperidin-2-one
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2009_10
CN(C)C(=O)c1c2c(c(O)c(=O)n1C)C(=O)N(Cc1ccc(F)c(Cl)c1)CC2
Reaction #1904532
6-(3-chloro-4-fluorobenzyl)-4-hydroxy-N,N,2-trimethyl-3,5-dioxo-2,3,5,6,7,8-hexahydro-2,6-naphthyridine-1-carboxamide
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2009_10
O=C1CCCCN1Cc1ccc(F)c(Cl)c1
Reaction #1904555
title product
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2009_10
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