3-hydroxyazetidine hydrochloride

OC1CN(CCCOCCc2ccc3ccsc3c2)C1
Reaction #7534
1-{3-[2-(1-benzothiophen-6-yl)ethoxy]propyl}-3-azetidinol
Ausbeute 24.5%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
OC1CN(CCCOCCc2ccc3sccc3c2)C1
Reaction #7536
1-{3-[2-(1-benzothiophen-5-yl)ethoxy]propyl}-3-azetidinol
Ausbeute 64.2%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
Cc1c(-c2ccccc2)c(F)c2oc(N3CC(O)C3)nc2c1C#N
Reaction #45696
7-Fluoro-2-(3-hydroxyazetidin-1-yl)-5-methyl-6-phenyl-1,3-benzoxazole-4-carbonitrile
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
Cl.O=c1c(-c2cccnc2)c[nH]n1-c1cc(N2CC(O)C2)ncn1
Reaction #66187
2-[6-(3-Hydroxyazetidin-1-yl)pyrimidin-4-yl]-4-pyridin-3-yl-1,2-dihydro-3H-pyrazol-3-one hydrochloride
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_09
—
Reaction #91824
solid
Ausbeute 91.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2016_09
O=C(Nc1cnn2ccc(N3CCC[C@@H]3c3cc(F)ccc3F)nc12)N1CC(O)C1
Reaction #92253
final product
Ausbeute 100.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2016_09
O=C(Nc1cnn2ccc(N3CC(F)(F)C[C@@H]3c3cccc(F)c3)nc12)N1CC(O)C1
Reaction #92266
final product
Ausbeute 48.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2016_09
O=C(Nc1cnn2ccc(N3CCC[C@@H]3c3cc(F)ccc3Cl)nc12)N1CC(O)C1
Reaction #92267
final product
Ausbeute 85.1%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2016_09
CC1(c2cccc(F)c2)CCCN1c1ccn2ncc(NC(=O)N3CC(O)C3)c2n1
Reaction #92272
final product
Ausbeute 55.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2016_09
O=C(Nc1cnn2ccc(N3CCC[C@@H]3c3cc(F)cc(Cl)c3)nc12)N1CC(O)C1
Reaction #92273
final product
Ausbeute 74.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2016_09
O=C(Nc1cnn2ccc(N3CCC[C@@H]3c3cc(F)ccc3C(F)F)nc12)N1CC(O)C1
Reaction #92274
final product
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2016_09
O=C(Nc1cnn2ccc(N3CCC[C@@H]3c3cccc(F)c3)nc12)N1CC(O)C1
Reaction #92286
final product
Ausbeute 96.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2016_09
COC(=O)c1cc(Cl)cnc1N1CC(O)C1
Reaction #159610
title compound ( D62 )
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_09
COC(=O)c1cc(Cl)cnc1N1CC(O)C1
Reaction #159611
title compound ( D62 )
Ausbeute 76.6%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_09
COC(=O)c1cc(C(F)(F)F)cnc1N1CC(O)C1
Reaction #159615
title compound ( D67 )
Ausbeute 82.6%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_09
COC(=O)c1cc(F)cnc1N1CC(O)C1
Reaction #159617
title compound ( D70 )
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_09
O=C(c1ccc2[nH]ncc2c1Nc1ccc(I)cc1F)N1CC(O)C1
Reaction #166253
title compound
Ausbeute 49.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_09
Cc1onc(-c2ccccc2)c1COc1ccc(C(=O)N2CC(O)C2)cn1
Reaction #170502
title compound
Ausbeute 91.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_09
COc1c(Cl)c(C)c(C(C)=O)c(OCCN2CC(O)C2)c1OCCCc1ccccc1
Reaction #306658
title compound
Ausbeute 16.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2012_06
O=C(c1ccc(F)c(F)c1Nc1ccc(I)cc1F)N1CC(O)C1
Reaction #324530
1-({3,4-difluoro-2-[(2-fluoro-4-iodophenyl)amino]phenyl}carbonyl)azetidin-3-ol
Ausbeute 88.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_02
Seite 1Weiter