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1292802

O=c1[nH]c(=O)n([C@H]2CC[C@@H](CO)O2)cc1I
Reaction #4984
iodide
Ausbeute 66.0%DOI: 10.6084/m9.figshare.5104873.v1
O=C(c1ccccc1)n1c(=O)[nH]cc(I)c1=O
Reaction #40947
title compound
Ausbeute 90.0%DOI: 10.6084/m9.figshare.5104873.v1
COC(CCn1cc(I)c(=O)n(C(=O)c2ccccc2)c1=O)OC
Reaction #40948
title compound
Ausbeute 91.8%DOI: 10.6084/m9.figshare.5104873.v1
O=C(c1ccccc1)n1c(=O)c(I)cn(CCCN2C[C@@H]3C[C@]3(c3ccc(C(F)(F)F)cc3)C2)c1=O
Reaction #40949
title compound
Ausbeute 84.9%DOI: 10.6084/m9.figshare.5104873.v1
O=c1[nH]c(=O)n(CCCN2C[C@@H]3C[C@]3(c3ccc(C(F)(F)F)cc3)C2)cc1I
Reaction #40950
title compound
Ausbeute 74.0%DOI: 10.6084/m9.figshare.5104873.v1
O=C(c1ccccc1)n1c(=O)c(I)cn(CCCCl)c1=O
Reaction #40951
title compound
Ausbeute 98.1%DOI: 10.6084/m9.figshare.5104873.v1
O=C(c1ccccc1)n1c(=O)c(-c2cccnc2)cn(CCCCl)c1=O
Reaction #40952
title compound
Ausbeute 20.3%DOI: 10.6084/m9.figshare.5104873.v1
O=C(c1ccccc1)n1c(=O)c(I)cn(CCCCCl)c1=O
Reaction #40954
title compound
Ausbeute 98.0%DOI: 10.6084/m9.figshare.5104873.v1
Cc1cc(-c2cn(CCCCCl)c(=O)n(C(=O)c3ccccc3)c2=O)ccn1
Reaction #40955
title compound
Ausbeute 25.1%DOI: 10.6084/m9.figshare.5104873.v1
Cc1ncccc1-c1cn(CCCCCl)c(=O)n(C(=O)c2ccccc2)c1=O
Reaction #40957
title compound
Ausbeute 66.4%DOI: 10.6084/m9.figshare.5104873.v1
O=C(c1ccccc1)n1c(=O)c(I)cn(CCCN2CC3CC3(c3ccc(Cl)cc3)C2)c1=O
Reaction #40986
1-{3-[1-(4-chlorophenyl)-3-azabicyclo[3.1.0]hex-3-yl]propyl}-5-iodo-3-(phenylcarbonyl)-2,4(1H,3H)-pyrimidinedione
DOI: 10.6084/m9.figshare.5104873.v1
O=c1[nH]c(=O)n(CCCN2CC3CC3(c3ccc(Cl)cc3)C2)cc1I
Reaction #40987
title compound
Ausbeute 83.6%DOI: 10.6084/m9.figshare.5104873.v1
O=C(c1ccccc1)n1c(=O)c(I)cn(CCCN2CC3CC3(c3cccc(C(F)(F)F)c3)C2)c1=O
Reaction #40988
title compound
Ausbeute 46.6%DOI: 10.6084/m9.figshare.5104873.v1
O=c1[nH]c(=O)n(CCCN2CC3CC3(c3cccc(C(F)(F)F)c3)C2)cc1I
Reaction #40989
title compound
Ausbeute 81.0%DOI: 10.6084/m9.figshare.5104873.v1
O=C(c1ccccc1)n1c(=O)[nH]cc(I)c1=O
Reaction #41025
title compound
Ausbeute 90.5%DOI: 10.6084/m9.figshare.5104873.v1
O=C(c1ccccc1)n1c(=O)c(I)cn(CCCCCl)c1=O
Reaction #41026
title compound
Ausbeute 98.0%DOI: 10.6084/m9.figshare.5104873.v1
O=C(c1ccccc1)n1c(=O)c(-c2cccnc2F)cn(CCCCCl)c1=O
Reaction #41027
title compound
Ausbeute 54.3%DOI: 10.6084/m9.figshare.5104873.v1
O=c1[nH]c(=O)n(CCCN2C[C@@H]3C[C@]3(c3ccc(C(F)(F)F)cc3)C2)cc1-c1ccccc1F
Reaction #41045
title compound
Ausbeute 76.6%DOI: 10.6084/m9.figshare.5104873.v1
O=c1[nH]c(=O)n(CCCN2C[C@@H]3C[C@]3(c3ccc(C(F)(F)F)cc3)C2)cc1-c1ccncc1
Reaction #41048
title compound
Ausbeute 32.0%DOI: 10.6084/m9.figshare.5104873.v1
—
Reaction #41064
base
Ausbeute 48.0%DOI: 10.6084/m9.figshare.5104873.v1
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