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1192825

Cl.O=C(NC1CN2CCC1CC2)c1cc2cc([N+](=O)[O-])ccc2s1
Reaction #43730
hydrochloride
Ausbeute 48.6%DOI: 10.6084/m9.figshare.5104873.v1
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)c1cc2cc([N+](=O)[O-])ccc2s1
Reaction #43745
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
Cl.O=C(N[C@@H]1CN2CCC1CC2)c1cc2cccc(Cl)c2s1
Reaction #43755
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
CS(=O)(=O)Nc1ccc2cc(C(=O)N[C@H]3CN4CCC3CC4)sc2c1.Cl
Reaction #43764
title compound
DOI: 10.6084/m9.figshare.5104873.v1
Cl.O=c1cnc2ccc(F)cc2n1CCN1CCC(NCc2cc3ccccc3s2)CC1
Reaction #68238
1-(2-(4-((benzo[b]thiophen-2-yl)methylamino)piperidin-1-yl)ethyl)-7-fluoroquinoxalin-2(1H)-one hydrochloride
DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc2ncc(=O)n(CCN3CCC(NCc4cc5ccccc5s4)CC3)c2c1.Cl
Reaction #68254
1-(2-(4-((benzo[b]thiophen-2-yl)methylamino)piperidin-1-yl)ethyl)-7-methoxyquinoxalin-2(1H)-one hydrochloride
DOI: 10.6084/m9.figshare.5104873.v1
O=C(NC1(C(=O)OCc2ccccc2)CCCCC1)c1cc2ccccc2s1
Reaction #161035
title compound
Ausbeute 91.0%DOI: 10.6084/m9.figshare.5104873.v1
O=C(NC1(C(=O)O)CCCCC1)c1cc2ccccc2s1
Reaction #161036
title compound
Ausbeute 83.8%DOI: 10.6084/m9.figshare.5104873.v1
O=C1OC(c2cc3ccccc3s2)=NC12CCCCC2
Reaction #161037
title compound
Ausbeute 76.7%DOI: 10.6084/m9.figshare.5104873.v1
CSCC[C@@H](C=O)NC(=O)C1(NC(=O)c2cc3ccccc3s2)CCCCC1
Reaction #161053
title compound
DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)[C@H](CCSC)NC(=O)C1(NC(=O)c2cc3ccccc3s2)CCCCC1
Reaction #161057
title compound
Ausbeute 86.4%DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc(F)c2cc(C#N)sc12
Reaction #176130
DOI: 10.1039/C8SC04228D
CC(C)Sc1c(C(N)=O)sc2ccccc12
Reaction #182258
DOI: 10.1039/C8SC04228D
CC(C)COC(C)ONC(=O)c1cc2ccc(CO)cc2s1
Reaction #188123
DOI: 10.1039/C8SC04228D
Cl
Reaction #188418
DOI: 10.1039/C8SC04228D
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