Teilstruktursuche

39610

O=C1OCC(CCN2CC(N3CCOCC3)C2)(c2ccc(Cl)c(Cl)c2)CN1CC1CCCCC1
Reaction #199043
DOI: 10.1039/C8SC04228D
C1CN(C2CNC2)CCO1.Cl.Cl
Reaction #464210
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CC(=O)N1CC(N2CCO[C@@H](CN3CCN(C(=O)Nc4ccc(Cl)c(Cl)c4)CC3)C2)C1
Reaction #690403
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CN(C[C@@H](CCN1CC(N2CCOCC2)C1)c1ccc(F)cc1)C(=O)c1cc(Br)cc(Br)c1.Cl.Cl
Reaction #836591
title compound
Ausbeute 119.7%DOI: 10.6084/m9.figshare.5104873.v1
CN(C[C@@H](CCN1CC(N2CCOCC2)C1)c1ccc(F)cc1)C(=O)c1cc(C#N)cc2c1CCCC2
Reaction #836593
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CN(C[C@@H](CCN1CC(N2CCOCC2)C1)c1ccc(F)cc1)C(=O)c1cc(Cl)cc(Cl)c1
Reaction #836595
title compound
Ausbeute 63.0%DOI: 10.6084/m9.figshare.5104873.v1
CNC[C@@H](CCN1CC(N2CCOCC2)C1)c1ccc(F)cc1.Cl.Cl
Reaction #836607
[(2S)-2-(4-fluorophenyl)-4-(3-morpholin-4-ylazetidin-1-yl)butyl]methylamine dihydrochloride
DOI: 10.6084/m9.figshare.5104873.v1
C1CN(C2CNC2)CCO1.Cl.Cl
Reaction #1153247
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)C[C@@H](CCCC1CCCCC1)c1nc(C(=O)N2CC(N3CCOCC3)C2)no1
Reaction #1367011
title compound
Ausbeute 105.9%DOI: 10.6084/m9.figshare.5104873.v1
CC1(N2CCOCC2)CNC1.Cl.Cl
Reaction #1453733
4-(3-methyl-3-azetidinyl)morpholine dihydrochloride
Ausbeute 74.9%DOI: 10.6084/m9.figshare.5104873.v1
C1CN(C2CNC2)CCO1.Cl.Cl
Reaction #1471979
title compound
DOI: 10.6084/m9.figshare.5104873.v1
O=C1OCC(CCN2CC(N3CCOCC3)C2)(c2ccc(Cl)c(Cl)c2)CN1CC1CCCCC1
Reaction #1544267
title compound
Ausbeute 74.1%DOI: 10.6084/m9.figshare.5104873.v1
C1CN(C2CNC2)CCO1.Cl.Cl
Reaction #1686619
title compound
DOI: 10.6084/m9.figshare.5104873.v1
C1CN(C2CNC2)CCO1.Cl.Cl
Reaction #1826926
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CCCS(=O)(=O)N1CC(CNC(=O)c2ccc(Cl)cc2Cl)(N2CCOCC2)C1
Reaction #2187501
2,4-dichloro-N-{[3-morpholin-4-yl-1-(propylsulfonyl)azetidin-3-yl]methyl}benzamide
Ausbeute 4.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)C[C@@H](CCCC1CCCCC1)c1nc(C(=O)N2CC(N3CCOCC3)C2)no1
Reaction #2270171
title compound
Ausbeute 105.9%DOI: 10.6084/m9.figshare.5104873.v1
CC(=O)N1CC(N2CCOC(CN3CCN(C(=O)Nc4ccc(Cl)c(Cl)c4)CC3)C2)C1
Reaction #2414319
DOI: 10.1039/C8SC04228D
CC(=O)N1CC(N2CCO[C@@H](CN3CCN(C(=O)Nc4ccc(Cl)c(Cl)c4)CC3)C2)C1
Reaction #2458360
title compound
DOI: 10.6084/m9.figshare.5104873.v1