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108504

Cc1c(Cl)c(C(F)(F)F)nn1CC(=O)N1CCCc2c1cnn2-c1ccc(F)cc1
Reaction #797798
title compound
DOI: 10.6084/m9.figshare.5104873.v1
Cc1cc(C(F)(F)F)nn1CC(=O)N1CCCc2c1cnn2-c1ccc(F)cc1
Reaction #797802
title compound
Ausbeute 67.0%DOI: 10.6084/m9.figshare.5104873.v1
Cc1c(Cl)c(C(F)(F)F)nn1C(C)C(=O)N1CCCc2c1cnn2-c1ccc(F)cc1
Reaction #797803
title compound
Ausbeute 75.0%DOI: 10.6084/m9.figshare.5104873.v1
Cc1nn(-c2ccc(F)cc2)c2c1N(C(=O)Cn1nc(C(F)(F)F)c(Cl)c1C)CCC2
Reaction #797804
title compound
Ausbeute 41.0%DOI: 10.6084/m9.figshare.5104873.v1
Cc1c(Cl)c(C(F)(F)F)nn1C(C)(C)C(=O)N1CCCc2c1cnn2-c1ccc(F)cc1
Reaction #797812
title compound
Ausbeute 68.0%DOI: 10.6084/m9.figshare.5104873.v1
CCC(C(=O)N1CCCc2c1cnn2-c1ccc(F)cc1)n1nc(C(F)(F)F)c(Cl)c1C
Reaction #797813
title compound
Ausbeute 69.0%DOI: 10.6084/m9.figshare.5104873.v1
Cc1c(Cl)c(C(F)(F)F)nn1C(C(=O)N1CCCc2c1cnn2-c1ccc(F)cc1)C(C)C
Reaction #797814
title compound
Ausbeute 74.0%DOI: 10.6084/m9.figshare.5104873.v1
Cc1c(Cl)c(C(F)(F)F)nn1CC(=O)N1CCCc2c1cnn2-c1ccc(F)cc1F
Reaction #797817
title compound
Ausbeute 70.0%DOI: 10.6084/m9.figshare.5104873.v1
CCC(C(=O)N1c2cnn(-c3ccc(F)cc3)c2CCC1C)n1nc(C(F)(F)F)cc1C
Reaction #797819
title compound
Ausbeute 46.0%DOI: 10.6084/m9.figshare.5104873.v1
Cc1cc(C(F)(F)F)nn1C(C)C(=O)N1CCCc2c1cnn2-c1ccc(F)cc1
Reaction #797822
desired product
Ausbeute 89.0%DOI: 10.6084/m9.figshare.5104873.v1
CCC(C(=O)N1CCCc2c1cnn2-c1ccc(F)cc1)n1nc(C(F)(F)F)cc1C
Reaction #797823
desired product
Ausbeute 92.0%DOI: 10.6084/m9.figshare.5104873.v1
O=C(Cn1nc(C(F)(F)F)c2c1CCOC2)N1CCCc2c1cnn2-c1ccc(F)cc1
Reaction #797836
desired product
Ausbeute 55.0%DOI: 10.6084/m9.figshare.5104873.v1
O=C(Cn1nc(C(F)(F)F)c2c1CCCC2)N1CCCc2c1cnn2-c1ccc(F)cc1
Reaction #797842
desired product
Ausbeute 55.0%DOI: 10.6084/m9.figshare.5104873.v1
COCC(C(=O)N1CCCc2c1cnn2-c1ccc(F)cc1)n1nc(C(F)(F)F)c(Cl)c1C
Reaction #797844
desired product
Ausbeute 12.0%DOI: 10.6084/m9.figshare.5104873.v1
Cc1c(Cl)c(C(F)(F)F)nn1C(CO)C(=O)N1CCCc2c1cnn2-c1ccc(F)cc1
Reaction #797845
desired product
Ausbeute 56.0%DOI: 10.6084/m9.figshare.5104873.v1
Cc1cc(C(F)(F)F)nn1C(CO)C(=O)N1CCCc2c1cnn2-c1ccc(F)cc1
Reaction #797846
desired product
Ausbeute 55.0%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)CC(C(=O)N1CCCc2c1cnn2-c1ccc(F)cc1)n1nc(C(F)(F)F)cc1C
Reaction #797847
ethyl 4-[1-(4-fluorophenyl)-6,7-dihydro-5H-pyrazolo[4,3-b]pyridin-4-yl]-3-[5-methyl-3-(trifluoromethyl)pyrazol-1-yl]-4-oxo-butanoate
Ausbeute 83.0%DOI: 10.6084/m9.figshare.5104873.v1
Cc1cc(C(F)(F)F)nn1C(CC1CCOCC1)C(=O)N1CCCc2c1cnn2-c1ccc(F)cc1
Reaction #797848
desired product
Ausbeute 6.0%DOI: 10.6084/m9.figshare.5104873.v1
Cc1cc(C(F)(F)F)nn1C(CC(=O)O)C(=O)N1CCCc2c1cnn2-c1ccc(F)cc1
Reaction #797849
4-[1-(4-fluorophenyl)-6,7-dihydro-5H-pyrazolo[4,3-b]pyridin-4-yl]-3-[5-methyl-3-(trifluoromethyl)pyrazol-1-yl]-4-oxo-butanoic acid
Ausbeute 103.9%DOI: 10.6084/m9.figshare.5104873.v1
Cc1cc(C(F)(F)F)nn1C(CC(N)=O)C(=O)N1CCCc2c1cnn2-c1ccc(F)cc1
Reaction #797850
desired product
Ausbeute 37.7%DOI: 10.6084/m9.figshare.5104873.v1
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