Ähnlichkeitssuche

41317

O=S(=O)(c1ccccc1C(F)(F)F)N1CCN2C[C@H](Oc3cnc(C4CC4)cn3)C[C@H]2C1
Reaction #327610
title compound
DOI: 10.6084/m9.figshare.5104873.v1
O=S(=O)(c1cccc(C(F)(F)F)c1)N1CCN2C[C@@H](Oc3cnc(C4CC4)cn3)C[C@H]2C1
Reaction #327619
title compound
DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc(S(=O)(=O)N2CCN3C[C@H](Oc4cnc(C5CC5)cn4)C[C@H]3C2)cc1C(C)(C)C
Reaction #327620
titled compound
DOI: 10.6084/m9.figshare.5104873.v1
CC(=O)c1cccc(S(=O)(=O)N2CCN3C[C@H](Oc4cnc(C5CC5)cn4)C[C@H]3C2)c1
Reaction #327624
title compound
Ausbeute 83.6%DOI: 10.6084/m9.figshare.5104873.v1
C=C(C)c1cnc(O[C@@H]2C[C@H]3CNCCN3C2)cn1.Cl
Reaction #327633
title compound
DOI: 10.6084/m9.figshare.5104873.v1
—
Reaction #327634
solid
Ausbeute 62.0%DOI: 10.6084/m9.figshare.5104873.v1
O=C1CCN(c2ccc(C(F)(F)F)cn2)C[C@H]2C[C@H](Oc3cnc(C4CC4)cn3)CN12
Reaction #659224
titled compound
Ausbeute 40.0%DOI: 10.6084/m9.figshare.5104873.v1
Cl.O=C1CCNC[C@H]2C[C@@H](Oc3cnc(C4CC4)cn3)CN12
Reaction #659226
(8R,9aR)-8-[(5-cyclopropylpyrazin-2-yl)oxy]octahydro-5H-pyrrolo[1,2-a][1,4]diazepin-5-one hydrochloride
DOI: 10.6084/m9.figshare.5104873.v1
O=C1CCN(Cc2ccc(OC(F)(F)F)cc2)C[C@H]2C[C@@H](Oc3cnc(C4CC4)cn3)CN12
Reaction #659227
title compound
Ausbeute 50.0%DOI: 10.6084/m9.figshare.5104873.v1
O=C(c1cccc(C(F)(F)F)c1)N1CCC(=O)N2C[C@H](Oc3cnc(C4CC4)cn3)C[C@@H]2C1
Reaction #659228
title compound
Ausbeute 64.0%DOI: 10.6084/m9.figshare.5104873.v1
O=C1CCN(S(=O)(=O)c2ccc(C(F)(F)F)cc2)C[C@H]2C[C@@H](Oc3cnc(C4CC4)cn3)CN12
Reaction #659229
title compound
Ausbeute 62.0%DOI: 10.6084/m9.figshare.5104873.v1
Cl.O=C1CCNC[C@@H]2C[C@H](Oc3cnc(C4CC4)cn3)CN12
Reaction #659232
title compound
Ausbeute 100.0%DOI: 10.6084/m9.figshare.5104873.v1
O=C1CCN(Cc2ccc(OC(F)(F)F)cc2)C[C@@H]2C[C@H](Oc3cnc(C4CC4)cn3)CN12
Reaction #659233
title compound
Ausbeute 46.4%DOI: 10.6084/m9.figshare.5104873.v1
O=C1CCN(Cc2ccc(OC(F)(F)F)cc2)C[C@H]2C[C@H](Oc3cnc(C4CC4)cn3)CN12
Reaction #659234
title compound
Ausbeute 53.0%DOI: 10.6084/m9.figshare.5104873.v1
O=C(c1cccc(C(F)(F)F)c1)N1CCC(=O)N2C[C@@H](Oc3cnc(C4CC4)cn3)C[C@@H]2C1
Reaction #659235
title compound
Ausbeute 54.7%DOI: 10.6084/m9.figshare.5104873.v1
O=C1CCN(S(=O)(=O)c2ccc(C(F)(F)F)cc2)C[C@H]2C[C@H](Oc3cnc(C4CC4)cn3)CN12
Reaction #659236
title compound
Ausbeute 56.0%DOI: 10.6084/m9.figshare.5104873.v1
O=C1CCN(c2ccc(C(F)(F)F)cn2)C[C@H]2C[C@H](Oc3cnc(C4CC4)cn3)CN12
Reaction #1137492
titled compound
Ausbeute 40.0%DOI: 10.6084/m9.figshare.5104873.v1
Cl.O=C1CCNC[C@H]2C[C@@H](Oc3cnc(C4CC4)cn3)CN12
Reaction #1137494
(8R,9aR)-8-[(5-cyclopropylpyrazin-2-yl)oxy]octahydro-5H-pyrrolo[1,2-a][1,4]diazepin-5-one hydrochloride
DOI: 10.6084/m9.figshare.5104873.v1
O=C1CCN(c2ccc(C(F)(F)F)cn2)C[C@H]2C[C@@H](Oc3cnc(C4CC4)cn3)CN12
Reaction #1137495
titled compound
Ausbeute 47.0%DOI: 10.6084/m9.figshare.5104873.v1
O=C1CCN(Cc2ccc(OC(F)(F)F)cc2)C[C@H]2C[C@@H](Oc3cnc(C4CC4)cn3)CN12
Reaction #1137496
title compound
Ausbeute 50.0%DOI: 10.6084/m9.figshare.5104873.v1
Seite 1Weiter