ethyl 4-amino-1-piperidine carboxylate

CCOC(=O)N1CCC(Nc2ccncc2)CC1
Reaction #48352
title compound
수율 41.1%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
CCOC(=O)N1CCC(NCc2cnccc2NC(=O)OC(C)(C)C)CC1
Reaction #48376
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
CCOC(=O)N1CCC(NCc2ccncc2NC(=O)OC(C)(C)C)CC1
Reaction #48378
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
CCOC(=O)N1CCC(Nc2ccc(C(=O)c3ccccc3F)c(N)n2)CC1
Reaction #58387
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2008_09
CCOC(=O)N1CCC(Nc2ccc(C(=O)c3cc(F)ccc3OC)c(N)n2)CC1
Reaction #58396
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2008_09
CCOC(=O)N1CCC(Nc2ccc(C(=O)c3c(OC)ccc(F)c3F)c(N)n2)CC1
Reaction #58416
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2008_09
CCOC(=O)N1CCC(Nc2ccc(C(=O)c3cc(F)c(C)cc3OC)c(N)n2)CC1
Reaction #58421
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2008_09
CCOC(=O)N1CCC(Nc2ccc(C(=O)c3cc(F)c(Cl)cc3OC)c(N)n2)CC1
Reaction #58425
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2008_09
CCOC(=O)N1CCCCC1N
Reaction #75874
amino-1-ethoxycarbonyl piperidine
수율 126.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2004_03
CCOC(=O)N1CCC(Nc2nc3ccccc3s2)CC1
Reaction #176323
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
CCOC(=O)N1CCC(Nc2c(C(=O)OC)c(=O)[nH]c3ccc(Cl)cc23)CC1
Reaction #186371
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
CCOC(=O)N1CCC(NCc2ccnc(-c3cc(OC)c(OC)c(OC)c3)c2)CC1
Reaction #199698
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
CCOC(=O)N1CCC(Nc2ncc3c(n2)N(C2CCCC2)CCC(=O)N3C)CC1
Reaction #204559
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
CCOC(=O)N1CCC(NC(=O)N2CCc3ccc(-c4cc(N5CCN(C)CC5)nc(N)n4)cc3C2)CC1
Reaction #225512
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
CCOC(=O)N1CCC(Nc2ccc(C(=O)c3ccccc3F)c(N)n2)CC1
Reaction #225544
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
CCOC(=O)N1CCC(NC(=O)c2ccccc2Oc2ccc(Cl)cc2Cl)CC1
Reaction #231684
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
CCOC(=O)N1CCC(NC(=O)c2ccc(-c3cc(F)cc(F)c3)nc2)CC1
Reaction #234138
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
CCOC(=O)N1CCC(Nc2cc(Cl)ccc2[N+](=O)[O-])CC1
Reaction #239010
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
CCOC(=O)N1CCC(Nc2ccc(C(=O)c3cc(F)ccc3OC)c(N)n2)CC1
Reaction #245658
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
CCOC(=O)N1CCC(Nc2nc3cccc(C(=O)OC)c3o2)CC1
Reaction #256988
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
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