4-hydroxyethyl piperidine

N=C(NC(=O)OCc1ccccc1)N1CCC(CCO)CC1
Reaction #955
title compound
Rendement 41.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
Cc1cc(C)c(S(=O)(=O)OCCC2CCN(S(=O)(=O)c3c(C)cc(C)cc3C)CC2)c(C)c1
Reaction #10570
N,O-Bis(2,4,6-trimethylbenzenesulfonyl)-4-piperidineethanol
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
CC(C)(C)OC(=O)n1c(-c2ccc(Cl)c3c2C(=O)NC3)cc2cc(CN3CCC(CCO)CC3)ccc21
Reaction #49303
4-chloro-7-{1-(tert-butoxycarbonyl)-5-[4-(2-hydroxyethyl)piperidinomethyl]indol-2-yl}isoindolinone
Rendement 110.3%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
OCCC1CCN(Cc2ccc(F)cc2)CC1
Reaction #82825
1-(4-fluorobenzyl)-4-(2-hydroxyethyl)piperidine
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1997_04
COc1cccc(C(=O)N2CCC(CCO)CC2)c1
Reaction #82828
2-[1-(3-methoxybenzoyl)piperidin-4-yl]ethanol
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1997_04
CC(C)(C)[Si](C)(C)OCCC1CCNCC1
Reaction #166361
compound 292
Rendement 86.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_09
O=C1CCc2cc(/C=C/C(=O)N3CCC(CCO)CC3)cnc2N1
Reaction #170093
title compound
Rendement 55.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_09
CCOc1ccccc1Cc1nc(N2CCC(CCO)CC2)c(C#N)c(=O)[nH]1
Reaction #176044
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
Cc1cc2nc(NC(=O)c3ccc(C(C)(C)O)cc3)cc(N3CCC(CCO)CC3)n2n1
Reaction #182922
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
CC(C)(C)OCCN1CCC(CCO)CC1
Reaction #191578
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
Cc1cccc(Cc2nc(N3CCC(CCO)CC3)c(C#N)c(=O)[nH]2)c1
Reaction #204589
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
O=C(OCc1ccccc1)N1CCC(CCO)CC1
Reaction #216691
captioned compound
Rendement 65.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1995_11
OCCC1CCN(c2cccc(Br)n2)CC1
Reaction #230180
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
CCN1CCC(CCO)CC1
Reaction #239021
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
CC(=O)Nc1nc(C)c(-c2csc(C(=O)N3CCC(CCO)CC3)n2)s1
Reaction #239654
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
COc1ccc(-c2ccccc2Cc2nc(N3CCC(CCO)CC3)c(C#N)c(=O)[nH]2)cn1
Reaction #247011
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
O=C(c1ccccc1)N1CCC(CCO)CC1
Reaction #268222
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (6/10)
OCCC1CCN(c2cncc3ccccc23)CC1
Reaction #285921
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (6/10)
Cc1nc(N2CCC(CCO)CC2)c2c(C)cn(-c3c(C)cc(Br)cc3C)c2n1
Reaction #294119
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (6/10)
OCCC1CCN(c2ccc3cc(Cl)ccc3n2)CC1
Reaction #296650
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (6/10)
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