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1292512

CN(C)CCCn1ccc2ccsc2c1=O
Reaction #189989
DOI: 10.1039/C8SC04228D
O=C(Nc1ccc(-n2ccc3cc(-c4ccc(Cl)cc4)sc3c2=O)cc1)C1CCNC1
Reaction #229864
DOI: 10.1039/C8SC04228D
COc1cc(-n2ccc3cc(-c4ccc(Cl)cc4)sc3c2=O)ccc1N1CCC(N(C)C)C1
Reaction #241917
DOI: 10.1039/C8SC04228D
COc1cc(-n2ccc3cc(-c4ccc(Cl)cc4)sc3c2=O)ccc1OC1CCCN(C)C1
Reaction #246926
DOI: 10.1039/C8SC04228D
N#Cc1ccc2c(c1)nc(Cl)c1sccc12
Reaction #252188
DOI: 10.1039/C8SC04228D
O=c1c2sc(-c3ccc(Cl)cc3)cc2ccn1-c1ccc(OC2CCNCC2)nc1
Reaction #405366
DOI: 10.1039/C8SC04228D
COC(=O)c1sc2c(c1N)c1ccsc1c(=O)n2-c1ccccc1
Reaction #433142
desired product
DOI: 10.6084/m9.figshare.5104873.v1
O=c1[nH]ccc2cc(-c3ccc(Cl)cc3)sc12
Reaction #510571
2-(4-chlorophenyl)-6H-thieno[2,3-c]pyridine-7-one
Ausbeute 100.0%DOI: 10.6084/m9.figshare.5104873.v1
CN(C)[C@H]1CCN(c2ccc(-n3ccc4cc(-c5ccc(Cl)cc5)sc4c3=O)cn2)C1.Cl
Reaction #510601
title compound
Ausbeute 116.4%DOI: 10.6084/m9.figshare.5104873.v1
O=c1c2sc(-c3ccc(Cl)cc3)cc2ccn1-c1ccc(OC2CCNCC2)nc1
Reaction #510602
2-(4-chloro-phenyl)-6-[6-(piperidin-4-yloxy)-pyridin-3-yl]-6H-thieno[2,3-c]pyridin-7-one
Ausbeute 73.4%DOI: 10.6084/m9.figshare.5104873.v1
CN1CCC(Oc2ccc(-n3ccc4cc(-c5ccc(Cl)cc5)sc4c3=O)cn2)CC1.Cl
Reaction #510604
title compound
Ausbeute 187.9%DOI: 10.6084/m9.figshare.5104873.v1
CC(=O)N1CCC(Oc2ccc(N3CCc4cc(-c5ccc(Cl)cc5)sc4C3=O)cn2)CC1
Reaction #510605
titled compound
Ausbeute 90.2%DOI: 10.6084/m9.figshare.5104873.v1
Cl.O=c1c2sc(-c3ccc(Cl)cc3)cc2ccn1-c1ccc(O[C@@H]2CCN(C3CC3)C2)nc1
Reaction #510606
desired product
Ausbeute 45.4%DOI: 10.6084/m9.figshare.5104873.v1
O=c1c2sc(-c3ccc(Cl)cc3)cc2ccn1-c1ccc(N2CC[C@@H](N3CC[C@@H](F)C3)C2)nc1
Reaction #510608
title compound
Ausbeute 71.0%DOI: 10.6084/m9.figshare.5104873.v1
N[C@@H]1CCN(c2ccc(-n3ccc4cc(-c5ccc(Cl)cc5)sc4c3=O)cn2)C1
Reaction #510609
6-[6-((R)-3-amino-pyrrolidin-1-yl)-pyridin-3-yl]-2-(4-chloro-phenyl)-6H-thieno[2,3-c]pyridin-7-one
Ausbeute 64.0%DOI: 10.6084/m9.figshare.5104873.v1
Cl.N[C@@H]1CCN(c2ccc(-n3ccc4cc(-c5ccc(Cl)cc5)sc4c3=O)cn2)C1
Reaction #510610
title compound
Ausbeute 93.0%DOI: 10.6084/m9.figshare.5104873.v1
CN(CC(F)F)[C@@H]1CCN(c2ccc(-n3ccc4cc(-c5ccc(Cl)cc5)sc4c3=O)cn2)C1
Reaction #510614
2-(4-chloro-phenyl)-6-(6-{(R)-3-[(2,2-difluoro-ethyl)-methyl-amino]-pyrrolidin-1-yl}-pyridin-3-yl)-6H-thieno[2,3-c]pyridin-7-one
Ausbeute 80.7%DOI: 10.6084/m9.figshare.5104873.v1
CN(CC(F)F)[C@@H]1CCN(c2ccc(-n3ccc4cc(-c5ccc(Cl)cc5)sc4c3=O)cn2)C1.Cl
Reaction #510615
title compound
Ausbeute 160.4%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)c1cc2c(Br)cn(C)c(=O)c2s1
Reaction #605664
title compound
Ausbeute 90.4%DOI: 10.6084/m9.figshare.5104873.v1
Cn1cc(Br)c2cc(C(N)=O)sc2c1=O
Reaction #605665
title compound
Ausbeute 95.0%DOI: 10.6084/m9.figshare.5104873.v1
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