4,4-difluoropiperidine hydrochloride

CC(C)N1CCC(NC(=O)c2nc3c(C(=O)N4CCC(F)(F)CC4)cccc3n2CC(=O)Nc2ccc(Cl)cn2)CC1
Reaction #46838
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
O=C1C=C(N2CCC(F)(F)CC2)C(c2ccc(N3CCOCC3)cc2)N1c1ccc2[nH]cnc2c1
Reaction #70056
1-(1H-Benzo[d]imidazol-5-yl)-4-(4,4-difluoropiperidin-1-yl)-5-(4-morpholinophenyl)-1H-pyrrol-2(5H)-one
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_09
CCC(C)[C@H](N)C(=O)N1CCC(F)(F)CC1.Cl
Reaction #78044
(S)-2-amino-1-(4,4-difluoro-piperidin-1-yl)-3-methyl-pentan-1-one hydrochloride
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2004_03
C[C@H](NC(=O)OC(C)(C)C)c1ccc(CN2CCC(F)(F)CC2)c(F)c1
Reaction #85672
Title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2016_09
FC1(F)CCN(Cc2cccc(Br)c2)CC1
Reaction #162766
title compound
Rendimiento 99.4%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_09
Cc1onc(-c2ccccc2)c1COc1ccc(C(=O)N2CCC(F)(F)CC2)cn1
Reaction #170341
title compound
Rendimiento 98.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_09
FC1(F)CCN(CCCOc2ccc(Br)cc2)CC1
Reaction #171403
title compound
Rendimiento 50.9%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_09
O=C(c1cc2cc(O)ccc2n1CC(F)(F)F)N1CCC(F)(F)CC1
Reaction #220010
title product
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2008_06
COc1c(Cl)c(C)c(C(C)=O)c(OCCN2CCC(F)(F)CC2)c1OCCC(C)c1ccc(F)cc1
Reaction #306641
title compound
Rendimiento 31.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2012_06
CC(C)(C)OC(=O)N1Cc2ccc(N3CCC(F)(F)CC3)cc2C1
Reaction #312770
5-(4,4-Difluoro-piperidin-1-yl)-1,3-dihydro-isoindole-2-carboxylic acid tert-butyl ester
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2009_07
N#Cc1nc2c(nc1N1CCC(F)(F)CC1)-c1ccccc1C2=O
Reaction #327491
8
Rendimiento 95.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_02
O=NN1CCC(F)(F)CC1
Reaction #340243
4,4-difluoro-1-nitrosopiperidine
Rendimiento 99.2%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2011_01
FC1(F)CCN(CC2(c3ccc(OCCCN4CCCC4)cc3)CCOCC2)CC1
Reaction #360060
title compound
Rendimiento 7.5%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2008_11
Cc1onc(-c2ccccc2)c1COc1ccc(C(=O)N2CCC(F)(F)CC2)cn1
Reaction #418940
title compound
Rendimiento 98.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_11
Cc1onc(-c2ccccc2)c1COc1ccc(C(=O)N2CCC(F)(F)CC2)cn1
Reaction #419443
title compound
Rendimiento 98.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_11
NC1=N[C@@]2(CO1)c1cc(-c3cccnc3F)ccc1Oc1cnc(N3CCC(F)(F)CC3)cc12
Reaction #423110
(S)-3-(4,4-difluoropiperidin-1-yl)-7-(2-fluoropyridin-3-yl)-5′H-spiro[chromeno[2,3-c]pyridine-5,4′-oxazol]-2′-amine
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_11
NC1=N[C@@]2(CO1)c1cc(-c3cccnc3F)ccc1Oc1c2cc(N2CCC(F)(F)C2)nc1F
Reaction #423184
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_11
NC1=N[C@@]2(CO1)c1cc(-c3cncc(F)c3)ccc1Oc1c2cc(N2CCC(F)(F)CC2)nc1F
Reaction #423187
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_11
NC1=N[C@@]2(CS1)c1cc(-c3cccnc3F)ccc1Oc1c(F)cc(N3CCC(F)(F)CC3)cc12
Reaction #423202
titled compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_11
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Reaction #487973
gum
Rendimiento 55.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_06
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