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128167

Cc1ccc(S(=O)(=O)n2cc(-c3ccc4[nH]ccc4c3)c3cc(Br)cnc32)cc1
Reaction #172195
title compound
Ausbeute 76.4%DOI: 10.6084/m9.figshare.5104873.v1
COc1cc(-c2cnc3[nH]cc(-c4ccc5[nH]ccc5c4)c3c2)cc(OC)c1OC
Reaction #172196
title compound
DOI: 10.6084/m9.figshare.5104873.v1
Nc1ncc(-c2cnc3[nH]cc(-c4cnc(N)nc4)c3c2)cn1
Reaction #172197
Compound W
DOI: 10.6084/m9.figshare.5104873.v1
CN(C)c1ccc(-c2cnc3[nH]cc(-c4ccc(N(C)C)nc4)c3c2)cn1
Reaction #172198
Compound X
DOI: 10.6084/m9.figshare.5104873.v1
Nc1ccc(-c2c[nH]c3ncc(-c4ccc(N)nc4)cc23)cc1
Reaction #172199
Compound Z
DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc(-c2cnc3[nH]cc(-c4ccc(C(N)=O)cc4)c3c2)cc1OC
Reaction #172200
4-(5-(3,4-dimethoxyphenyl)-1H-pyrrolo[2,3-b]pyridin-3-yl)benzamide
DOI: 10.6084/m9.figshare.5104873.v1
COc1cc(-c2cnc3[nH]cc(-c4ccc(C(N)=O)cc4)c3c2)ccc1N
Reaction #172201
4-(5-(4-amino-3-methoxyphenyl)-1H-pyrrolo[2,3-b]pyridin-3-yl)benzamide
DOI: 10.6084/m9.figshare.5104873.v1
NC(=O)c1ccc(-c2c[nH]c3ncc(-c4ccc(N)nc4)cc23)cc1
Reaction #172202
4-(5-(6-aminopyridin-3-yl)-1H-pyrrolo[2,3-b]pyridin-3-yl)benzamide
DOI: 10.6084/m9.figshare.5104873.v1
Cc1ccc(S(=O)(=O)n2cc(-c3ccc4[nH]ccc4c3)c3cc(-c4ccc(C=O)cc4)cnc32)cc1
Reaction #172203
4-(3-(1H-indol-5-yl)-1-tosyl-1H-pyrrolo[2,3-b]pyridin-5-yl)benzaldehyde
DOI: 10.6084/m9.figshare.5104873.v1
COc1cc(-c2cnc3[nH]cc(-c4ccc5[nH]ccc5c4)c3c2)ccc1OCCN1CCNCC1
Reaction #172205
title compound
DOI: 10.6084/m9.figshare.5104873.v1
COc1cc(-c2cnc3[nH]cc(-c4ccc5[nH]ccc5c4)c3n2)ccc1OCCN1CCOCC1
Reaction #172213
4-(2-(4-(7-(1H-indol-5-yl)-5H-pyrrolo[3,2-b]pyrazin-2-yl)-2-methoxyphenoxy)ethyl)morpholine
DOI: 10.6084/m9.figshare.5104873.v1
CC(=O)N1CCN(Cc2ccc(-c3cnc4[nH]cc(-c5ccc6[nH]ccc6c5)c4c3)cc2)CC1
Reaction #172231
title compound
Ausbeute 46.0%DOI: 10.6084/m9.figshare.5104873.v1
CN1CCN(C(=O)c2ccc(-c3cnc4[nH]cc(-c5ccc6[nH]ccc6c5)c4c3)cc2)CC1
Reaction #172232
title compound
Ausbeute 28.0%DOI: 10.6084/m9.figshare.5104873.v1
Cc1ccc(S(=O)(=O)n2cc(-c3ccc4[nH]ccc4c3)c3cc(-c4ccc(C=O)cc4)cnc32)cc1
Reaction #172249
title compound
Ausbeute 88.5%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)N1CCN(Cc2ccc(-c3cnc4[nH]cc(-c5ccc6[nH]ccc6c5)c4c3)cc2)CC1
Reaction #172252
title compound
Ausbeute 35.1%DOI: 10.6084/m9.figshare.5104873.v1
CN1CCN(Cc2ccc(-c3cnc4[nH]cc(-c5ccc(O)cc5)c4c3)cc2)CC1
Reaction #172260
title compound
DOI: 10.6084/m9.figshare.5104873.v1
Cc1[nH]c2ncc(-c3ccc(CN4CCN(C)CC4)cc3)cc2c1-c1ccc2[nH]ccc2c1
Reaction #172270
title compound
DOI: 10.6084/m9.figshare.5104873.v1
Cc1[nH]c2ncc(-c3ccc(CN4CCN(C)CC4)cc3)cc2c1-c1ccc(O)cc1
Reaction #172272
title compound
DOI: 10.6084/m9.figshare.5104873.v1
Cc1ccc(S(=O)(=O)n2cc(-c3ccc4[nH]ccc4c3)c3cc(Br)cnc32)cc1
Reaction #420320
title compound
Ausbeute 76.4%DOI: 10.6084/m9.figshare.5104873.v1
COc1cc(-c2cnc3[nH]cc(-c4ccc5[nH]ccc5c4)c3c2)cc(OC)c1OC
Reaction #420321
title compound
DOI: 10.6084/m9.figshare.5104873.v1
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