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830598

CCCc1nc2cc(N(Cc3ccc(OC(F)(F)F)cc3)S(=O)(=O)c3ccc(F)cc3)ccc2n1CC(=O)O
Reaction #43845
title compound
DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)c1ccc(OCCCO/N=C/c2ccc(-c3ccccc3)cc2)cc1NC(=O)c1ccc(OC(F)(F)F)cc1
Reaction #57955
4-[3-({[(1E)-1,1′-biphenyl-4-ylmethylidene]amino}oxy)propoxy]-2-{[4-(trifluoromethoxy)benzoyl]amino}benzoic acid methyl ester
Ausbeute 80.0%DOI: 10.6084/m9.figshare.5104873.v1
O=C(Nc1cc(OCCCO/N=C/c2ccc(-c3ccccc3)cc2)ccc1C(=O)O)c1ccc(OC(F)(F)F)cc1
Reaction #57956
4-[3-({[(1E)-1,1′-biphenyl-4-ylmethylidene]amino}oxy)propoxy]-2-{[4-(trifluoromethoxy)benzoyl]amino}benzoic acid
Ausbeute 96.4%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)c1ccc(OCCCO/N=C/c2ccc(C(F)(F)F)cc2)cc1NC(=O)c1ccc(OC(F)(F)F)cc1
Reaction #57957
2-{[4-(trifluoromethoxy)benzoyl]amino}-4-{3-[({(1E)-[4-(trifluoromethyl)phenyl]methylidene}amino)oxy]propoxy}benzoic acid methyl ester
Ausbeute 78.0%DOI: 10.6084/m9.figshare.5104873.v1
O=C(Nc1cc(OCCCO/N=C/c2ccc(-c3ccccc3)cc2)ccc1C(=O)O)c1ccc(OC(F)(F)F)cc1
Reaction #57958
4-[3-({[(1E)-1,1′-biphenyl-4-ylmethylidene]amino}oxy)propoxy]-2-{[4-(trifluoromethoxy)benzoyl]amino}benzoic acid
Ausbeute 192.8%DOI: 10.6084/m9.figshare.5104873.v1
O=C(Nc1cccnc1)N1CCN(Cc2ccc3c(c2)OC(F)(F)O3)CC1
Reaction #68878
title compound
DOI: 10.6084/m9.figshare.5104873.v1
O=C(Nc1cccnc1)N1CCN(Cc2ccc3c(c2)OC(F)(F)O3)CC1
Reaction #68879
title compound
DOI: 10.6084/m9.figshare.5104873.v1
O=C(Nc1ccncc1)N1CCN(Cc2ccc3c(c2)OC(F)(F)O3)CC1
Reaction #68880
title compound
DOI: 10.6084/m9.figshare.5104873.v1
O=C(Nc1ccncn1)N1CCN(Cc2ccc3c(c2)OC(F)(F)O3)CC1
Reaction #68882
title compound
DOI: 10.6084/m9.figshare.5104873.v1
O=C(Nc1c(Cl)cncc1Cl)c1ccc(OC(F)F)c(OCC2CC2)c1
Reaction #70958
Roflumilast
DOI: 10.6084/m9.figshare.5104873.v1
CC(C#N)(Cn1nc2cc(Cl)cc(CO)c2n1)NC(=O)c1ccc(OC(F)(F)F)cc1
Reaction #158146
title compound
Ausbeute 67.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(C#N)(Cn1nc2cc(Cl)cc(CN)c2n1)NC(=O)c1ccc(OC(F)(F)F)cc1
Reaction #158149
title compound
Ausbeute 87.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(C#N)(Cn1nc2cc(C(F)(F)F)cc(C#N)c2n1)NC(=O)c1ccc(OC(F)(F)F)cc1
Reaction #158150
title compound
Ausbeute 63.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(C#N)(Cn1nc2cc(Cl)cc(-c3ccc(C(F)(F)F)cc3)c2n1)NC(=O)c1ccc(OC(F)(F)F)cc1
Reaction #158151
title compound
DOI: 10.6084/m9.figshare.5104873.v1
COc1c2c(C)cc(C(N)=O)cc2nn1CC(C)(C#N)NC(=O)c1ccc(OC(F)(F)F)cc1
Reaction #158170
title compound
DOI: 10.6084/m9.figshare.5104873.v1
NC(=O)c1cc2c(OCC(O)CN3CCN(C(c4ccccc4)c4ccc(OC(F)F)cc4)CC3)cccc2[nH]1
Reaction #177139
DOI: 10.1039/C8SC04228D
CC(C#N)(Cn1cc2ncc(Br)cc2n1)NC(=O)c1ccc(OC(F)(F)F)cc1F
Reaction #180381
DOI: 10.1039/C8SC04228D
Cc1cc(C=O)cc2c1C(=O)N(Cc1ccc(OC(F)(F)F)cc1)C2
Reaction #180963
DOI: 10.1039/C8SC04228D
O=C1c2c(Cl)cc(OCC(F)F)cc2CN1Cc1ccc(OC(F)(F)F)cc1
Reaction #187173
DOI: 10.1039/C8SC04228D
Nc1ccc2oc3c(OC(F)F)ccc(C(=O)Nc4c(Cl)cncc4Cl)c3c2c1
Reaction #187386
DOI: 10.1039/C8SC04228D
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