3-methylpiperidine

CC1CCCN(Cc2cccc(O)c2)C1
Reaction #4744
3-[(3-Methylpiperidin-1-yl)methyl]phenol
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1988_02
CC1CCCN(C(=O)[C@H](C)N2CC[C@H](NS(=O)(=O)c3ccc4cc(Cl)ccc4c3)C2=O)C1
Reaction #7397
title compound
Ausbeute 27.3%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
CC1CCCN(C(=O)[C@@H](C)N2CC[C@H](NS(=O)(=O)c3ccc4cc(Cl)ccc4c3)C2=O)C1
Reaction #7403
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
CC#CCOc1ncnc(N2CCCC(C)C2)c1F
Reaction #42793
4-(2-butynyloxy)-5-fluoro-6-(3-methylpiperidino) pyrimidine
Ausbeute 94.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
CCC#CCOc1ncnc(N2CCCC(C)C2)c1F
Reaction #42799
5-fluoro-4-(3-methylpiperidino)-6-(2-pentynyloxy)pyrimidine
Ausbeute 89.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
CC#CCOc1cc(N2CCCC(C)C2)ncn1
Reaction #42806
4-(2-butynyloxy)-6-(3-methylpiperidino) pyrimidine
Ausbeute 73.9%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
CC1CCCN(Sc2nc3ccccc3s2)C1
Reaction #54172
1-(2-benzothiazolylthio)-3-methyl-piperidine
Ausbeute 95.5%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1979_04
CC1CCCN(C[C@@H]2COc3ccc(S(C)(=O)=O)cc3O2)C1
Reaction #67182
3-METHYL-1-{[(2R)-7-(METHYLSULFONYL)-2,3-DIHYDRO-1,4-BENZODIOXIN-2-YL]METHYL}PIPERIDINE
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_09
CC#CCOc1cc(N2CCCC(C)C2)ncn1
Reaction #177308
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
CC#CCOc1ncnc(N2CCCC(C)C2)c1F
Reaction #183777
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
CCC#CCOc1ncnc(N2CCCC(C)C2)c1F
Reaction #192947
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
CC1CCCN(c2ccc([N+](=O)[O-])cc2C(=O)c2ccc(Cl)cc2)C1
Reaction #195805
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
CC1CCCN(Cc2ccc(Oc3ccc(C(N)=O)cn3)cc2)C1
Reaction #217957
title compound
Ausbeute 29.5%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2008_06
CC(=Cc1sccc1C)C1(C)OCC(CN2CCCC(C)C2)O1
Reaction #224910
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
CC1CCCN(C(=O)c2nc(-c3ccccc3)nc3ccccc23)C1
Reaction #231877
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
CC1CCCN(C(=O)C(C)N2CCC(NS(=O)(=O)c3ccc4cc(Cl)ccc4c3)C2=O)C1
Reaction #280711
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (6/10)
CC1CCCN(Cc2ccc(Oc3ccc(C(N)=O)cn3)cc2)C1
Reaction #315415
title compound
Ausbeute 29.5%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2009_07
CC1CCCN(CCNc2ccnc3cc(Cl)ccc23)C1
Reaction #321871
colourless crystals
Ausbeute 64.3%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1997_01
CC1CCCN(CCCC#N)C1
Reaction #334229
4-(3-methylpiperidino)-butyronitrile
Ausbeute 70.3%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1987_11
CC1CCCN(c2c(Br)cc3c4c(cccc24)C(=O)N(OCc2ccccc2)C3=O)C1
Reaction #366147
title compound
Ausbeute 86.9%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2002_03
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