trans-2-amino-cyclopentanol hydrochloride

C#C[C@H]1CC[C@@H](C#N)N1C(=O)CNC1CCC[C@@H]1O
Reaction #562578
titled compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_01
CCn1c(=O)c2c(nc(NC3CCCC3O)n2Cc2ccc(OC)c(Br)c2)n(CCO)c1=O
Reaction #595005
Compound 13A
Ausbeute 85.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_08
O=C1c2cc(Cc3ccc(-n4cccn4)cc3)c(C3CC3)cc2CN1[C@@H]1CCC[C@H]1O
Reaction #716535
title compound
Ausbeute 49.9%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2016_04
O[C@@H]1CCC[C@H]1N(Cc1ccccc1)Cc1ccccc1
Reaction #805191
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2015_11
C#C[C@H]1CC[C@@H](C#N)N1C(=O)CNC1CCC[C@@H]1O
Reaction #943051
titled compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2007_08
Cn1c(N[C@@H]2CCC[C@H]2O)nccc1=O
Reaction #1269843
product
Ausbeute 76.5%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_03
C#C[C@H]1CC[C@@H](C#N)N1C(=O)CNC1CCC[C@@H]1O
Reaction #1380581
titled compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2007_07
O[C@@H]1CCC[C@H]1N(Cc1ccccc1)Cc1ccccc1
Reaction #1493226
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_12
Cn1c(N[C@@H]2CCC[C@H]2O)nc2n[nH]c(Nc3ccccc3)c2c1=O
Reaction #1565596
crude product
Ausbeute 85.7%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2016_08
C#C[C@H]1CC[C@@H](C#N)N1C(=O)CNC1CCC[C@@H]1O
Reaction #1729896
titled compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2012_02
CCCCCCCCCC(=O)CC(=O)N[C@@H]1CCC[C@H]1O
Reaction #1869154
N-(trans-2- hydroxycyclopentyl)-3-oxododecanamide
Ausbeute 54.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2009_03
CCn1c(=O)c2c(nc(NC3CCCC3O)n2Cc2ccc(OC)c(Br)c2)n(CCO)c1=O
Reaction #1879278
Compound 13A
Ausbeute 85.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_07
CCOCn1c(-c2nc(N[C@@H]3CCC[C@H]3O)ncc2Cl)cc2c(C(=O)NC3CC3)cccc21
Reaction #1973922
2-{5-chloro-2-[(1R,2R)-2-hydroxycyclopentylamino]pyrimidin-4-yl}-N-cyclopropyl-1-(ethoxymethyl)-1H-indole-4-carboxamide
Ausbeute 93.6%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_08
CCCCc1noc(C)c1/C=C/c1nc(C)c(C(=O)N[C@@H]2CCC[C@H]2O)s1
Reaction #2010809
title compound
Ausbeute 75.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2012_05
Cc1onc(-c2ccccn2)c1COc1ccc(C(=O)N[C@H]2CCC[C@@H]2O)nc1
Reaction #2050151
title compound
Ausbeute 78.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_04
N#Cc1ccc2c(c1)cc(C(=O)N[C@@H]1CCC[C@H]1O)n2Cc1cccc(OC(F)(F)F)c1
Reaction #2329549
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_03
O=C(N[C@@H]1CCC[C@H]1O)C(O)=CC(=O)c1cc(Cc2ccc(F)cc2F)cn(Cc2ccccc2F)c1=O
Reaction #2455979
titled compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_04
Cn1c(N[C@@H]2CCC[C@H]2O)nc2n[nH]c(Nc3ccccc3)c2c1=O
Reaction #2476639
crude product
Ausbeute 85.7%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2012_09