Participa en 23 reacciones

790477

CN1CCCCC1CN1C[C@H](CCCB(O)O)[C@](N)(C(=O)O)C1
Reaction #89659
(3R,4S)-3-amino-4-(3-boronopropyl)-1-((1-methylpiperidin-2-yl)methyl)pyrrolidine-3-carboxylic acid
Rendimiento 74.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2016_09
CN1CCCCC1COS(C)(=O)=O
Reaction #314551
(1-methylpiperidin-2-yl)methyl methanesulfonate
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2009_07
CN1CCCCC1COc1ccccc1N1CCN(C(=O)OC(C)(C)C)CC1
Reaction #369785
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (8/10)
CN1CCCCC1COc1ccccc1N1CCN(C(=O)OC(C)(C)C)CC1
Reaction #543624
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2007_03
CN1CCCC[C@@H]1CO
Reaction #544425
(R)-(+)-1-Methyl-2-piperidinemethanol
Rendimiento 15.6%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2007_03
CN1CCCCC1COC(=O)C1CCCCN1C
Reaction #570660
N-Methyl-(2-piperidyl)methyl N-Methylpipecolinate
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1993_07
CN(C)CC(=O)OCC1CCCCN1C
Reaction #570661
N-methyl-2-piperidylmethyl N,N-dimethylaminoacetate
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1993_07
CN1CCCCC1CN1C[C@H](CCCB(O)O)[C@](N)(C(=O)O)C1
Reaction #677907
(3R,4S)-3-amino-4-(3-boronopropyl)-1-((1-methylpiperidin-2-yl)methyl)pyrrolidine-3-carboxylic acid
Rendimiento 74.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2016_01
CN1CCCCC1CCl
Reaction #922887
DOI: 10.1039/C8SC04228DTest data from https://doi.org/10.1039/C8SC04228D
CN(C)CCn1ccc2ccc(C3(O)CCOCC3)cc21
Reaction #931423
6-(4-hydroxy-tetrahydropyran-4-yl)-1-(2-(N,N-dimethylamino)ethyl)-1H-indole
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2002_04
CN1CCCCC1COC(=O)c1c[nH]c2ccccc12
Reaction #980456
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1992_06
C1CCNCC1.CCOCC.c1ccc2[nH]ccc2c1
Reaction #1053680
indole piperidine ether
Rendimiento 40.4%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2005_10
CN(C)CCn1ccc2ccc(C3(O)CCOCC3)cc21
Reaction #1075280
6-(4-hydroxy-tetrahydropyran-4-yl)-1-(2-(N,N-dimethylamino)ethyl)-1H-indole
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2003_10
C[N+]1(C)CCCCC1CO.Cc1ccc(S(=O)(=O)[O-])cc1
Reaction #1175741
desired compound
Rendimiento 157.1%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1990_10
CN1CCCCC1C=O
Reaction #1484245
1-methylpiperidine-2-carbaldehyde
Rendimiento 31.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_12
COC(=O)[C@@H](OC(C)(C)C)c1c(C)c(C(C)O)c2nc3cn2c1N1CCC(C)(CC1)OCCCC[C@H](C)Oc1ccc(F)c(F)c1-c1cccc-3c1
Reaction #1569299
Methyl(2S)-2-(tert-butoxy)-2-[(22S)-16,17-difluoro-5-(1-hydroxyethyl)-4,22,28-trimethyl-21,27-dioxa-1,7,34-triazahexacyclo[26.2.2.16,9.110,14.02,7.015,20]tetratriaconta-2,4,6(34),8,10(33),11,13,15(20),16,18-decaen-3-yl]acetate
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2016_08
Cc1ccc(S(=O)(=O)OCC2CCCCN2C)cc1
Reaction #1617703
(1-methylpiperidin-2-yl)methyl 4-methylbenzenesulfonate
Rendimiento 36.5%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2015_07
CN1CCCC[C@@H]1CO
Reaction #1848183
alcohol
Rendimiento 15.6%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2005_01
CN1CCCCC1COc1cc(N)ncc1C#N
Reaction #1865084
(racemic) 6-amino-4-((1-methylpiperidin-2-yl)methoxy)nicotinonitrile
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2016_02
C[N+]1(C)CCCCC1CO.Cc1ccc(S(=O)(=O)[O-])cc1
Reaction #2168677
desired compound
Rendimiento 157.1%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1993_02
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