(S)-2-chloro-5-(2-(pyrrolidin-2-yl)-1H-imidazol-5-yl)pyrimidine trihydrochloride

O=C(Cc1cccnc1)N1CCC[C@H]1c1ncc(-c2cnc(Cl)nc2)[nH]1
Reaction #49150
title compound
Yield 25.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
O=C(Cc1cccnc1)N1CCC[C@H]1c1ncc(-c2cnc(Cl)nc2)[nH]1
Reaction #325100
title compound
Yield 25.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_02
O=C(Cc1cccnc1)N1CCC[C@H]1c1ncc(-c2cnc(Cl)nc2)[nH]1
Reaction #541154
title compound
Yield 25.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_07
O=C(Cc1cccnc1)N1CCC[C@H]1c1ncc(-c2cnc(Cl)nc2)[nH]1
Reaction #676128
title compound
Yield 25.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2016_01
O=C(Cc1cccnc1)N1CCC[C@H]1c1ncc(-c2cnc(Cl)nc2)[nH]1
Reaction #1483178
title compound
Yield 25.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_12
O=C(Cc1cccnc1)N1CCC[C@H]1c1ncc(-c2cnc(Cl)nc2)[nH]1
Reaction #1529805
title compound
Yield 25.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_02
O=C(Cc1cccnc1)N1CCC[C@H]1c1ncc(-c2cnc(Cl)nc2)[nH]1
Reaction #1563221
title compound
Yield 25.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2015_04
O=C(Cc1cccnc1)N1CCC[C@H]1c1ncc(-c2cnc(Cl)nc2)[nH]1
Reaction #1571444
title compound
Yield 25.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2016_08
O=C(Cc1cccnc1)N1CCC[C@H]1c1ncc(-c2cnc(Cl)nc2)[nH]1
Reaction #1961068
title compound
Yield 25.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2012_11
Clc1ncc(-c2cnc[nH]2)cn1.O=CC(c1cccnc1)N1CCCC1
Reaction #2122542
title compound
Yield 25.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_11
Clc1ncc(-c2cnc[nH]2)cn1.O=CC(c1cccnc1)N1CCCC1
Reaction #2153253
title compound
Yield 25.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2012_10
O=C(Cc1cccnc1)N1CCC[C@H]1c1ncc(-c2cnc(Cl)nc2)[nH]1
Reaction #2279060
title compound
Yield 25.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2012_12
O=C(Cc1cccnc1)N1CCC[C@H]1c1ncc(-c2cnc(Cl)nc2)[nH]1
Reaction #2444528
title compound
Yield 25.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_07