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Nc1ccc(Cl)nc1I

Nc1ccc(Cl)nc1I
Reaction #40583
expected product
Ausbeute 39.1%DOI: 10.6084/m9.figshare.5104873.v1
—
Reaction #40587
solid
Ausbeute 33.0%DOI: 10.6084/m9.figshare.5104873.v1
Cc1cc(Cl)nc(I)c1N
Reaction #178474
DOI: 10.1039/C8SC04228D
Nc1ccc(Cl)nc1I
Reaction #196584
DOI: 10.1039/C8SC04228D
CCOC(=O)C(C)(C)CC#Cc1nc(Cl)ccc1N
Reaction #199658
DOI: 10.1039/C8SC04228D
Cc1cc(Cl)nc(-c2ccco2)c1N
Reaction #286105
DOI: 10.1039/C8SC04228D
Nc1ccc(Cl)nc1I
Reaction #312933
expected product
Ausbeute 39.1%DOI: 10.6084/m9.figshare.5104873.v1
—
Reaction #312937
solid
Ausbeute 33.0%DOI: 10.6084/m9.figshare.5104873.v1
Nc1ccc(Cl)nc1I
Reaction #600245
6-chloro-2-iodo-pyridin-3-ylamine
Ausbeute 86.4%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)C#Cc1nc(Cl)ccc1N
Reaction #600246
6-chloro-2-(3,3-dimethyl-but-1-ynyl)-pyridin-3-ylamine
Ausbeute 88.0%DOI: 10.6084/m9.figshare.5104873.v1
Nc1ccc(Cl)nc1-c1ncccc1F
Reaction #721723
6-chloro-3′-fluoro-[2,2′-bipyridin]-3-amine
Ausbeute 69.0%DOI: 10.6084/m9.figshare.5104873.v1
Nc1ccc(Cl)nc1I
Reaction #838622
desired product
DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)C(C)(C)CC#Cc1nc(Cl)ccc1N
Reaction #838623
desired product
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)C#Cc1nc(Cl)ccc1N
Reaction #903079
DOI: 10.1039/C8SC04228D
Cc1cc(Cl)nc(I)c1N
Reaction #974893
title compound
Ausbeute 54.3%DOI: 10.6084/m9.figshare.5104873.v1
Cc1cc(Cl)nc(-c2ccco2)c1N
Reaction #974894
title compound
Ausbeute 86.6%DOI: 10.6084/m9.figshare.5104873.v1
Nc1ccc(Cl)nc1I
Reaction #974907
title compound
Ausbeute 80.8%DOI: 10.6084/m9.figshare.5104873.v1
Nc1ccc(Cl)nc1-c1ccco1
Reaction #974908
title compound
Ausbeute 0.1%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)CCc1c(-c2ccc(Cl)cc2)[nH]c2ccc(Cl)nc12
Reaction #1103820
Methyl 5-Chloro-2-(4-chlorophenyl)-1H-pyrrolo[3,2-b]pyridine-3-propanoate
DOI: 10.6084/m9.figshare.5104873.v1
Nc1ccc(Cl)nc1I
Reaction #1131177
6-chloro-2-iodo-pyridin-3-ylamine
Ausbeute 86.4%DOI: 10.6084/m9.figshare.5104873.v1
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