4-piperidone hydrochloride monohydrate

O=C1CCN(c2ncc(-c3ccccc3Cl)nn2)CC1
Reaction #93481
6-(2-Chlorophenyl)-3-(4-oxopiperidino)-1,2,4-triazine
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1986_09
O=C1CCN(C(=O)c2ccc(Cl)cc2)CC1
Reaction #216260
title compound
Rendimiento 74.6%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1995_11
O=C1CCN(C(=O)c2ccc(Cl)cc2)CC1
Reaction #216261
N-(4-Chlorobenzoyl)-4-piperidone
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1995_11
CS(=O)(=O)N1CCC(=O)CC1
Reaction #220091
white solid
Rendimiento 87.1%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2008_06
C1=C(c2c[nH]c3ccccc23)CCNC1
Reaction #314448
final product
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2009_07
Fc1ccc2c(C3CCNCC3)c[nH]c2c1
Reaction #314457
6-fluoro-3-piperidin-4-yl-1H-indole
Rendimiento 51.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2009_07
CS(=O)(=O)N1CCC(=O)CC1
Reaction #358944
white solid
Rendimiento 87.1%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2008_11
O=C1CCN(CC2CC2)CC1
Reaction #359739
title compound
Rendimiento 55.3%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2008_11
O=C1CC(C(=O)c2ccc(F)cc2F)CCN1
Reaction #366106
product
Rendimiento 71.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2002_03
Cl.c1ccc(C2(c3ccccc3)CCNCC2)cc1
Reaction #409290
off-white solid
Rendimiento 72.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2001_04
O=C1CC(C(=O)c2ccc(F)cc2F)CCN1
Reaction #411516
product
Rendimiento 71.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2001_04
COC(=O)CCN1CCC(=O)CC1
Reaction #466274
title compound
Rendimiento 42.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2001_10
COc1cc2ncc(C#N)c(Nc3ccc(F)c(Cl)c3)c2cc1NC(=O)C=CCN1CCC(O)(O)CC1
Reaction #466374
4-(4,4-Dihydroxy-piperidin-1-yl)-but-2-enoic Acid[4-(3-chloro-4-fluoro-phenylamino)-3-cyano-7-methoxy-quinolin-6-yl]-amide
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2001_10
CC(C)(C)OC(=O)N1CCC(=O)CC1
Reaction #468578
N-t-butyloxycarbonyl-4-piperidone
Rendimiento 40.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2001_10
Cl.c1ccc(C2(c3ccccc3)CCNCC2)cc1
Reaction #469840
off-white solid
Rendimiento 72.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2001_10
COCCN1CCC(=O)CC1
Reaction #478239
1-(2-methoxy-ethyl)piperidin-4-one
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_02
COc1cc(-c2cc(CN3CCC(=O)CC3)ccn2)cc(OC)c1OC
Reaction #482611
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2003_08
Cl.c1ccc(C2(c3ccccc3)CCNCC2)cc1
Reaction #483785
off-white solid
Rendimiento 72.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2003_08
O=C1CCN(C(c2ccccc2)(c2ccccc2)c2ccccc2)CC1
Reaction #484787
1-triphenylmethyl-4-piperidone
Rendimiento 103.5%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2003_08
C1=C(c2c(-c3ccccc3)[nH]c3ccccc23)CCNC1
Reaction #516367
title compound
Rendimiento 73.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2001_11
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