4-methoxypiperidine

COC1CCN(C/C=C/C(=O)N2CCc3c(sc4ncnc(Nc5cc(O)cc(Cl)c5)c34)C2)CC1
Reaction #66884
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_09
COC1CCN(c2ccc3c(c2)CCN(c2ccc(N4CC[C@@H](N(C)C)C4)c(F)c2)C3=O)CC1
Reaction #156597
2-[4-((R)-3-Dimethylaminopyrrolidin-1-yl)-3-fluorophenyl]-6-(4-methoxypiperidin-1-yl)-3,4-dihydro-2H-isoquinolin-1-one
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_09
COC1CCN(C(=O)[C@@H]2CCCN(c3cccc(-c4nc5ccccc5n4C)c3)C2)CC1
Reaction #164287
title compound
Ausbeute 77.1%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_09
COC1CCN(CCOc2n[nH]c3ncnc(Nc4ccc(OCc5ccccn5)c(Cl)c4)c23)CC1
Reaction #185050
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
COC1CCN(CCCN2C(=O)c3ccccc3C2=O)CC1
Reaction #191396
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
Cl
Reaction #195345
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
COC1CCN(Cc2cccc(C#CCCN3CCOCC3)c2)CC1
Reaction #221291
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
COc1cc([N+](=O)[O-])ccc1OCCN1CCC(OC)CC1
Reaction #221650
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
COC1CCN(C(=O)Cl)CC1
Reaction #224898
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
COC1CCN(S(=O)(=O)c2ccc(S(N)(=O)=O)c(Cl)c2)CC1
Reaction #229752
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
Cl
Reaction #280099
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (6/10)
COc1ccc(N2CCC(OC)CC2)c2sc(NC(=O)N3CCOCC3)nc12
Reaction #280257
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (6/10)
COC1CCN(C(=O)c2cc3cc(C(=O)N4CCN(C(C)C)CC4)ccc3[nH]2)CC1
Reaction #293296
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (6/10)
C=C1CCN(c2ccc(Cl)cc2)C1=O
Reaction #294479
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (6/10)
COC1CCN(C(=O)c2noc3c(F)c(N4C[C@@H](C)O[C@@H](C)C4)c(CO[Si](c4ccccc4)(c4ccccc4)C(C)(C)C)cc23)CC1
Reaction #332651
(5-((tert-butyldiphenylsilyloxy)methyl)-6-((2R,6S)-2,6-dimethylmorpholino)-7-fluorobenzo[d]isoxazol-3-yl)(4-methoxypiperidin-1-yl)methanone
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_02
COC(=O)c1cccc2oc(N3CCC(OC)CC3)nc12
Reaction #337065
methyl 2-(4-methoxypiperidin-1-yl)benzoxazole-4-carboxylate
Ausbeute 50.8%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2011_01
COC1CCN(Cc2cccc(C#CCCN3CCOCC3)c2)CC1
Reaction #355809
4-{4-[3-(4-Methoxy-piperidin-1-ylmethyl)-phenyl]-but-3-ynyl}-morpholine
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2008_11
COC1CCN(CCCCl)CC1
Reaction #360005
title compound
Ausbeute 60.2%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2008_11
COC1CCN(C2=NC(=O)C(=Cc3ccc4c(cnn4Cc4ccc(Cl)cc4C(F)(F)F)c3)S2)CC1
Reaction #369041
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (8/10)
COC(=O)CCC(C(N)=O)N1Cc2c(OCc3ccc(CN4CCC(OC)CC4)cc3)cccc2C1=O
Reaction #382701
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (8/10)
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