4-phenyl-4-hydroxypiperidine

C[C@H](OC(=O)[C@@H](c1ccccc1)N1CCC(O)(c2ccccc2)CC1)c1ccccc1
Reaction #46643
title compound
수율 27.3%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
CC(C)(C)OC(=O)n1c(-c2ccc(Cl)c3c2C(=O)NC3)cc2cc(CN3CCC(O)(c4ccccc4)CC3)ccc21
Reaction #49334
4-chloro-7-[1-(tert-butoxycarbonyl)-5-(4-hydroxy-4-phenylpiperidinomethyl)indol-2-yl]isoindolinone
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
COc1cc2oc(=O)ccc2cc1OCC(O)CN1CCC(O)(c2ccccc2)CC1
Reaction #50600
(±)-6-[2-hydroxy-3-(4-hydroxy-4-phenyl-1-piperidinyl)propoxy]-7-methoxy-2H-1-benzopyran-2-one
수율 69.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1995_06
ClCCl.N
Reaction #62008
ammonia DCM
수율 1.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2008_09
OC1(c2ccccc2)CCN(CCC2COc3ccccc3O2)CC1
Reaction #94232
2-[2-(4-hydroxy-4-phenylpiperidino)-ethyl]-1,4-benzodioxan
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1978_12
OC1(c2ccccc2)CCN(CCC2Cc3ccccc3O2)CC1
Reaction #94235
2-[2-(4-hydroxy-4-phenylpiperidino)-ethyl]-2,3-dihydrobenzofuran
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1978_12
O=C(CC1COc2ccccc2O1)N1CCC(O)(c2ccccc2)CC1
Reaction #94238
1-[2-(1,4-benzodioxan-2-yl)-acetyl]-4-hydroxy-4-phenylpiperidine
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1978_12
Cl.OC1(c2ccccc2)CCN(CCC2COc3ccccc3O2)CC1
Reaction #94240
2-[2-(4-hydroxy-4-phenylpiperidino)ethyl]-1,4-benzodioxan hydrochloride
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1978_12
O=C(N1CCC(O)(c2ccccc2)CC1)C(F)(F)F
Reaction #94247
1-trifluoroacetyl-4-hydroxy-4-phenylpiperidine
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1978_12
C=C(C#N)CN1CCC(O)(c2ccccc2)CC1
Reaction #94931
2-[(4-Hydroxy-4-phenyl-1-piperidyl)methyl]propenenitrile
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1982_08
C=C(C#N)CN1CCC(O)(c2ccccc2)CC1
Reaction #94941
2-[(4-Hydroxy-4-phenyl-1-piperidyl)methyl]propenenitrile
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1982_08
O=C1CCc2cc(/C=C/C(=O)N3CCC(O)(c4ccccc4)CC3)cnc2N1
Reaction #170118
title compound
수율 41.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_09
CC(C)(C)OC(=O)c1ccc(N2CCC(O)(c3ccccc3)CC2)cc1
Reaction #178017
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
OC1(c2ccccc2)CCN(CCC2COc3ccccc3O2)CC1
Reaction #182779
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
Cl
Reaction #190125
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
CC(C)(O)c1ccc2c(c1)C(=CCCN1CCC(O)(c3ccccc3)CC1)c1cccnc1CO2
Reaction #198089
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
COc1cc(OC)c2c(C)c(CCN3CCC(O)(c4ccccc4)CC3)c(=O)oc2c1
Reaction #203934
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
Cc1ccc(NC(=O)c2ccc(N3CCC(O)(c4ccccc4)CC3)nc2)cc1I
Reaction #207436
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
C=C(C#N)CN1CCC(O)(c2ccccc2)CC1
Reaction #214023
2-[(4-Hydroxy-4-phenyl-1-piperidyl)methyl]propenenitrile
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1981_03
Cl
Reaction #222323
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
1 페이지다음 페이지