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1390160

O=C(NC1CCCCC1O)c1nc(-c2ccc(Cl)c(Cl)c2)c(Oc2ccccc2)nc1C(F)(F)F
Reaction #182681
DOI: 10.1039/C8SC04228D
O=C(NC1CCCCC1O)c1nc(-c2ccc(Cl)c(Cl)c2)c(OCC(F)(F)F)nc1C(F)(F)F
Reaction #200583
DOI: 10.1039/C8SC04228D
O=C(O)c1nc(-c2ccc(Cl)cc2)c(Br)nc1C(F)(F)F
Reaction #212019
DOI: 10.1039/C8SC04228D
CC(C)Cc1cc(NC(=O)c2nccnc2C(F)(F)F)ccc1C(C(F)(F)F)C(F)(F)F
Reaction #375420
DOI: 10.1039/C8SC04228D
CC(Cc1ccc(Cl)cc1Cl)NC(=O)c1nccnc1C(F)(F)F
Reaction #476356
desired compound
Ausbeute 63.1%DOI: 10.6084/m9.figshare.5104873.v1
O=C(N[C@@H]1CCCC[C@H]1O)c1nc(-c2ccc(Cl)cc2)c(Br)nc1C(F)(F)F
Reaction #503650
title compound
Ausbeute 82.9%DOI: 10.6084/m9.figshare.5104873.v1
O=C(O)c1nc(-c2ccc(Cl)cc2)c(Br)nc1C(F)(F)F
Reaction #503651
title compound
Ausbeute 74.6%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)c1nc(-c2ccc(Cl)cc2)c(Br)nc1C(F)(F)F
Reaction #503652
title compound
Ausbeute 91.0%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)c1nc(-c2ccc(Cl)cc2)c(N)nc1C(F)(F)F
Reaction #503653
title compound
DOI: 10.6084/m9.figshare.5104873.v1
O=C(N[C@@H]1CCCC[C@H]1O)c1nc(-c2cccc(Cl)c2)c(Br)nc1C(F)(F)F
Reaction #503658
5-bromo-6-(3-chloro-phenyl)-3-trifluoromethyl-pyrazine-2-carboxylic acid ((1R,2R)-2-hydroxy-cyclohexyl)-amide
DOI: 10.6084/m9.figshare.5104873.v1
O=C(N[C@@H]1CCCC[C@H]1O)c1nc(-c2ccc(Cl)c(Cl)c2)c(OCC(F)(F)F)nc1C(F)(F)F
Reaction #503661
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CC(O)(CNC(=O)c1nc(-c2ccc(Cl)c(Cl)c2)c(OCC2CC2)nc1C(F)(F)F)C1CC1
Reaction #503662
title compound
DOI: 10.6084/m9.figshare.5104873.v1
O=C(N[C@@H]1CCCC[C@H]1O)c1nc(-c2ccc(Cl)c(Cl)c2)c(Oc2ccccc2)nc1C(F)(F)F
Reaction #503663
title compound
DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)c1nccnc1C(F)(F)F
Reaction #622967
title compound
Ausbeute 41.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)C1C2CCC1c1c(NC(=O)c3nccnc3C(F)(F)F)cccc12
Reaction #622968
title compound
Ausbeute 80.4%DOI: 10.6084/m9.figshare.5104873.v1
O=C(NCC1(c2ncc(Br)cc2Cl)CC1)c1nccnc1C(F)(F)F
Reaction #666055
3-trifluoromethyl-pyrazine-2-carboxylic acid [1-(5-bromo-3-chloro-pyridin-2-yl)-cyclopropylmethyl]-amide
Ausbeute 91.3%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)c1nccnc1C(F)(F)F
Reaction #692005
desired compound
Ausbeute 29.3%DOI: 10.6084/m9.figshare.5104873.v1
O=C(O)c1nccnc1C(F)(F)F
Reaction #692006
desired compound
Ausbeute 63.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)Cc1cc(NC(=O)c2nccnc2C(F)(F)F)ccc1C(C(F)(F)F)C(F)(F)F
Reaction #692007
desired compound
Ausbeute 62.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(O)(CNC(=O)c1nc(-c2ccc(Cl)c(Cl)c2)c(OCC2CC2)nc1C(F)(F)F)C1CC1
Reaction #765575
DOI: 10.1039/C8SC04228D
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