2-methylpiperidine

CC#CCOc1ncnc(N2CCCCC2C)c1F
Reaction #42791
4-(2-butynyloxy)-5-fluoro-6-(2-methylpiperidino)pyrimidine
Rendement 71.1%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
CC#CCOc1cc(N2CCCCC2C)ncn1
Reaction #42807
4-(2-butynyloxy)-6-(2-methylpiperidino)pyrimidine
Rendement 27.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
CC(Nc1ncnc2cc(C(=O)N3CCCCC3C)c(Cl)cc12)c1nc2cc(Cl)ccc2[nH]1
Reaction #62470
6-chloro-4-[(1R/S)-1-(5-chloro-1H-benzimidazol-2-yl)-ethylamino]-7-[(2R/S)-2-methyl-piperidin-1-yl-carbonyl]-quinazoline
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2008_09
CC1CCCCN1c1ccc([N+](=O)[O-])cc1C(=O)c1ccc(Cl)cc1
Reaction #180607
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
CC1CCCCN1c1ccc(Br)cc1C=O
Reaction #181476
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
CC1CCCCN1CCN1CCC(NC(=O)OC(C)(C)C)CC1
Reaction #188528
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
CC1CCCCN1c1ccc(C#N)c2ccccc12
Reaction #193543
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
CC1CCCCN1C(=O)Cn1c2c(c3cc(Cl)ccc31)CN(C)CC2
Reaction #201028
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
CC1CCCCN1CCC(=O)N1c2ccc(Cl)cc2NC(=O)c2ccccc21
Reaction #226325
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
CC1CCCCN1c1c(-c2c(F)cc(F)cc2F)c(Cl)nc2nccn12
Reaction #230190
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
CCOC(=O)c1ccc(N2CCCCC2C)c([N+](=O)[O-])c1
Reaction #306964
ethyl 4-(2-methylpiperidin-1-yl)-3-nitrobenzoate
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2012_06
CC1CCCCN1c1ccc(C(=O)O)cc1C#N
Reaction #306983
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2012_06
CC1CCCCN1c1ccc(C(=O)O)cc1[N+](=O)[O-]
Reaction #306984
title compound
Rendement 80.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2012_06
CC1CCCCN1c1ccc(C(=O)O)cc1[N+](=O)[O-]
Reaction #306999
title compound
Rendement 80.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2012_06
CC1CCCCN1c1ccc(Br)cc1C=O
Reaction #307052
title compound
Rendement 89.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2012_06
CC1CCCCN1c1ccc(C(F)(F)F)cc1[N+](=O)[O-]
Reaction #371104
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (8/10)
COC1=C(OC)C(=O)C(Cc2ccc(Oc3ccccc3)c(C(=O)N3CCCCC3C)c2)=C(C)C1=O
Reaction #388140
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (8/10)
CC1CCCCN1C(=O)c1cc(Cl)cc(OCCN(C(=O)OC(C)(C)C)c2ccncc2)c1
Reaction #401212
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (8/10)
CC1CCCCN1CCc1cc2cc(-c3ccc(C#N)cc3)ccc2o1
Reaction #403819
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (8/10)
CC1CCCCN1c1ccc(C(=O)O)cc1[N+](=O)[O-]
Reaction #423411
title compound
Rendement 94.4%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_11
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