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776541

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
O=C(c1cccc(C(F)(F)F)c1)N1CCC(=O)N2C[C@H](Oc3cnc(C4CC4)cn3)C[C@@H]2C1
Reaction #1137497
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 #1137498
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 #1137501
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 #1137502
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 #1137503
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 #1137504
title compound
Ausbeute 54.7%DOI: 10.6084/m9.figshare.5104873.v1
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