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236

CCOC(=O)c1cnc(Nc2cc(Cl)ccn2)o1
Reaction #447
Ausbeute 0.0%
CCOC(=O)c1cnc(Nc2cc(Cl)ccn2)o1
Reaction #448
Ausbeute 0.0%
CC(=O)Nc1cc(Nc2cc(NC3CC3)n3ncc(C#N)c3n2)ccc1N1CC[C@@H](N)C1
Reaction #466
Ausbeute 17.8%
CC(=O)Nc1cc(Nc2cc(NC3CC3)n3ncc(C#N)c3n2)c(F)cc1C
Reaction #702
Ausbeute 20.6%
CC(=O)Nc1cc(Nc2cc(NC3CC3)n3ncc(C#N)c3n2)ccc1N(C)CCN(C)C
Reaction #711
Ausbeute 15.6%
CC(=O)Nc1cc(Nc2cc(NC3COC3)n3ncc(C#N)c3n2)c(F)cc1C1CC1
Reaction #790
Ausbeute 23.9%
CC(=O)Nc1cc(Nc2cc(NC3COC3)n3ncc(C#N)c3n2)c(F)cc1C1CC1
Reaction #791
Ausbeute 11.9%
CC(=O)Nc1cc(Nc2cc(NC3COC3)n3ncc(C#N)c3n2)c(F)cc1C1CC1
Reaction #792
Ausbeute 3.5%
CC(=O)Nc1cc(Nc2cc(NC3CC3)n3ncc(C#N)c3n2)ncc1C
Reaction #821
Ausbeute 10.6%
CC(=O)Nc1cc(Nc2cc(NC3COC3)n3ncc(C#N)c3n2)ccc1C
Reaction #824
Ausbeute 16.5%
CC(=O)Nc1cc(Nc2cc(NC3COC3)n3ncc(C#N)c3n2)ccc1C1CC1
Reaction #832
Ausbeute 7.0%
CC(=O)Nc1cc(Nc2cc(NC3COC3)n3ncc(C#N)c3n2)ccc1C1CC1
Reaction #833
Ausbeute 0.0%
CC(=O)Nc1cc(Nc2cc(NC3COC3)n3ncc(C#N)c3n2)ccc1C1CC1
Reaction #834
Ausbeute 8.7%
Cc1cn(-c2cc(F)c([C@H](C)N)cc2F)cn1
Reaction #85724
(S)-1-(2,5-difluoro-4-(4-methyl-1H-imidazol-1-yl)phenyl)ethanamine
Ausbeute 143.4%DOI: 10.6084/m9.figshare.5104873.v1
COc1c(-c2ccc3cc(NS(C)(=O)=O)ccc3c2)cc(-n2ccc(=O)[nH]c2=O)cc1C(C)(C)C
Reaction #86681
title compound
Ausbeute 73.0%DOI: 10.6084/m9.figshare.5104873.v1
COc1c(-c2ccc3cc(NS(C)(=O)=O)ccc3c2)cc(-n2ccc(=O)[nH]c2=O)cc1C(C)(C)C
Reaction #86682
title compound
Ausbeute 94.6%DOI: 10.6084/m9.figshare.5104873.v1
COc1c(-c2ccc3cc(NS(C)(=O)=O)ccc3c2)cc(-n2ccc(=O)[nH]c2=O)cc1C(C)(C)C
Reaction #86683
Solid
Ausbeute 167.8%DOI: 10.6084/m9.figshare.5104873.v1
COc1c(-c2ccc3cc(NS(C)(=O)=O)ccc3c2)cc(-n2ccc(=O)[nH]c2=O)cc1C(C)(C)C
Reaction #86684
N-(6-(3-tert-butyl-5-(2,4-dioxo-3,4-dihydropyrimidin-1(2H)-yl)-2-methoxyphenyl)naphthalen-2-yl)methanesulfonamide
DOI: 10.6084/m9.figshare.5104873.v1
—
Reaction #86685
solid
Ausbeute 89.0%DOI: 10.6084/m9.figshare.5104873.v1
—
Reaction #86686
solid
Ausbeute 88.0%DOI: 10.6084/m9.figshare.5104873.v1
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