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Cl.Cl.Nc1ccc2sc(C(=O)NC3CN4CCC3CC4)cc2c1
Reaction #43731
title compound
DOI: 10.6084/m9.figshare.5104873.v1
Cl.O=C(N[C@H]1CN2CCC1CC2)c1sc2ccccc2c1Cl
Reaction #43748
title compound
DOI: 10.6084/m9.figshare.5104873.v1
Cl.O=C(N[C@@H]1CN2CCC1CC2)c1sc2ccccc2c1Cl
Reaction #43749
title compound
DOI: 10.6084/m9.figshare.5104873.v1
Cl.Cl.Nc1ccc2sc(C(=O)N[C@H]3CN4CCC3CC4)cc2c1
Reaction #43750
title compound
DOI: 10.6084/m9.figshare.5104873.v1
Cl.Cl.Nc1ccc2sc(C(=O)N[C@@H]3CN4CCC3CC4)cc2c1
Reaction #43751
title compound
DOI: 10.6084/m9.figshare.5104873.v1
Cc1c(C(=O)N[C@H]2CN3CCC2CC3)sc2ccc(N)cc12.Cl.Cl
Reaction #43752
title compound
DOI: 10.6084/m9.figshare.5104873.v1
Cl.Cl.Nc1cccc2cc(C(=O)N[C@H]3CN4CCC3CC4)sc12
Reaction #43753
title compound
DOI: 10.6084/m9.figshare.5104873.v1
Cl.O=C(N[C@H]1CN2CCC1CC2)c1cc2cccc(Cl)c2s1
Reaction #43754
title compound
DOI: 10.6084/m9.figshare.5104873.v1
Cl.O=C(N[C@@H]1CN2CCC1CC2)c1cc2cccc(Cl)c2s1
Reaction #43755
title compound
DOI: 10.6084/m9.figshare.5104873.v1
Cl.O=C(Nc1ccc2sc(C(=O)N[C@H]3CN4CCC3CC4)cc2c1)c1ccco1
Reaction #43756
title compound
DOI: 10.6084/m9.figshare.5104873.v1
Cl.O=C(Nc1ccc2sc(C(=O)N[C@H]3CN4CCC3CC4)cc2c1)c1ccccc1
Reaction #43757
title compound
DOI: 10.6084/m9.figshare.5104873.v1
Cl.Cl.Nc1ccc2c(Cl)c(C(=O)N[C@H]3CN4CCC3CC4)sc2c1
Reaction #43759
title compound
DOI: 10.6084/m9.figshare.5104873.v1
Cl.Cl.N/C(=N\O)c1ccc2cc(C(=O)N[C@H]3CN4CCC3CC4)sc2c1
Reaction #43761
title compound
DOI: 10.6084/m9.figshare.5104873.v1
Cl.Cl.N/C(=N\O)c1cccc2cc(C(=O)N[C@H]3CN4CCC3CC4)sc12
Reaction #43767
title compound
DOI: 10.6084/m9.figshare.5104873.v1
O=C(N[C@@H]1CCCN2c3cc(Cl)ccc3Oc3ccccc3[C@H]12)OCCl
Reaction #44437
trans-(7-chloro-2,3,4,14b-tetrahydro-1H-dibenzo[b,f]pyrido[1,2-d][1,4]oxazepin-1-yl)carbamic acid chloromethyl ester
Ausbeute 88.0%DOI: 10.6084/m9.figshare.5104873.v1
O=C(N[C@@H]1CCCN2c3c(ccc(Cl)c3Cl)Oc3ccccc3[C@H]12)C(F)(F)F
Reaction #44440
trans-N-(6,7-dichloro-2,3,4,14b-tetrahydro-1H-dibenzo[b,f]pyrido[1,2-d][1,4]oxazepin-1-yl)-2,2,2-trifluoroacetamide
Ausbeute 17.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(=O)N[C@@H]1CCCN2c3c(ccc(Cl)c3Cl)Oc3ccccc3[C@H]12
Reaction #44447
title compound
Ausbeute 36.4%DOI: 10.6084/m9.figshare.5104873.v1
COCCN[C@@H]1CCCN2c3c(ccc(Cl)c3Cl)Oc3ccccc3[C@H]12
Reaction #44448
crude title compound
Ausbeute 100.0%DOI: 10.6084/m9.figshare.5104873.v1
O=CN[C@@H]1CCCN2c3c(ccc(Cl)c3Cl)Oc3ccccc3[C@H]12
Reaction #44449
title compound
Ausbeute 30.0%DOI: 10.6084/m9.figshare.5104873.v1
O=C(N[C@@H]1C[C@H]2CCN(C2)C1)c1cn2cccc2cn1
Reaction #53436
N-[(3R,5R)-1-azabicyclo[3.2.1]oct-3-yl]pyrrolo[1,2-a]pyrazine-3-carboxamide
Ausbeute 83.0%DOI: 10.6084/m9.figshare.5104873.v1
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