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1312102

COC(=O)c1ccc([N+](=O)[O-])cc1NC(=O)c1ccc(OC(F)(F)F)cc1
Reaction #57951
4-nitro-2-(4-trifluoromethoxy-benzoylamino)-benzoic acid methyl ester
Ausbeute 70.0%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)c1ccc(O)cc1NC(=O)c1ccc(OC(F)(F)F)cc1
Reaction #57952
4-hydroxy-2-(4-trifluoromethoxy-benzoylamino)-benzoic acid methyl ester
Ausbeute 83.0%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)c1ccc(OCCCBr)cc1NC(=O)c1ccc(OC(F)(F)F)cc1
Reaction #57953
4-(3-bromo-propoxy)-2-(4-trifluoromethoxy-benzoylamino)-benzoic acid methyl ester
Ausbeute 75.0%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)c1ccc(OCCCO/N=C/c2cc(C(F)(F)F)cc(C(F)(F)F)c2)cc1NC(=O)c1ccc(OC(F)(F)F)cc1
Reaction #57954
4-{3-[({(1E)-[3,5-bis(trifluoromethyl)phenyl]methylidene}amino)oxy]propoxy}-2-{[4-(trifluoromethoxy)benzoyl]amino}benzoic acid methyl ester
Ausbeute 94.0%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(NC1CCN(C(=O)c2ccc(OC(F)(F)F)cc2)CC1)c1ccc(F)cc1
Reaction #78063
4-(4-fluorobenzoylamino)-1-(4-trifluoromethoxybenzoyl)piperidine
DOI: 10.6084/m9.figshare.5104873.v1
CC1(N2Cc3cc(CNC(=O)c4ccc(OC(F)(F)F)cc4)ccc3C2=O)CCC(=O)NC1=O
Reaction #91698
N-[2-(3-methyl-2,6-dioxo-piperidin-3-yl)-1-oxo-2,3-dihydro-1H-isoindol-5-ylmethyl]-4-trifluoromethoxy-benzamide
Ausbeute 71.9%DOI: 10.6084/m9.figshare.5104873.v1
CC(C#N)(Cn1nc2ccc(Cl)cc2n1)NC(=O)c1ccc(OC(F)(F)F)cc1
Reaction #158103
title compound
Ausbeute 55.6%DOI: 10.6084/m9.figshare.5104873.v1
CC(C#N)(Cn1nc2cc(Cl)cc(C=O)c2n1)NC(=O)c1ccc(OC(F)(F)F)cc1
Reaction #158144
title compound
Ausbeute 79.0%DOI: 10.6084/m9.figshare.5104873.v1
CN(C)Cc1cc(Cl)cc2nn(CC(C)(C#N)NC(=O)c3ccc(OC(F)(F)F)cc3)nc12
Reaction #158145
title compound
Ausbeute 52.0%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(C(=O)O)c2n1)NC(=O)c1ccc(OC(F)(F)F)cc1
Reaction #158147
title compound
Ausbeute 87.0%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)c1cc(Cl)cc2nn(CC(C)(C#N)NC(=O)c3ccc(OC(F)(F)F)cc3)nc12
Reaction #158148
title compound
Ausbeute 40.0%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
COc1c2ccc(N)cc2nn1CC(C)(C#N)NC(=O)c1ccc(OC(F)(F)F)cc1
Reaction #158168
title compound
Ausbeute 64.2%DOI: 10.6084/m9.figshare.5104873.v1
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