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642733

Cc1cc(N2CCC(=CC(=O)O)CC2)c2cccc(-c3ccc(Cl)cc3Cl)c2n1
Reaction #51829
2-{1-[8-(2,4-dichlorophenyl)-2-methylquinolin-4-yl]-piperidin-4-ylidene}acetic acid
DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)C1(COc2ccc3c(c2)CN(C(=O)OC(C)(C)C)CC3)CCN(c2ccncc2)CC1
Reaction #221914
DOI: 10.1039/C8SC04228D
O=C(O)C1CCN(c2ccncc2)CC1
Reaction #282124
DOI: 10.1039/C8SC04228D
CCOC(=O)C1CCN(c2ccncc2)CC1
Reaction #286854
DOI: 10.1039/C8SC04228D
CCOC(=O)C1CCN(c2ccncc2)CC1
Reaction #368659
DOI: 10.1039/C8SC04228D
CCOC(=O)C1CCN(c2cc(C)nc3c2c(C)cn3-c2c(C)cc(Cl)cc2C)CC1
Reaction #389918
DOI: 10.1039/C8SC04228D
CCOC(=O)C1CCN(c2cc(C)nc3ccccc23)CC1
Reaction #421118
brown oil
Ausbeute 162.9%DOI: 10.6084/m9.figshare.5104873.v1
OCC1CCN(c2ccnc3ccccc23)CC1
Reaction #499697
title compound
Ausbeute 88.0%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)C1(COc2ccc3c(c2)CN(C(=O)OC(C)(C)C)CC3)CCN(c2ccncc2)CC1
Reaction #499705
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)C1(COc2ccc3c(c2)CNCC3)CCN(c2ccncc2)CC1
Reaction #499706
title compound
Ausbeute 95.6%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)C1(COc2ccc3c(c2)CN(C(=N)N)CC3)CCN(c2ccncc2)CC1.Cl.Cl
Reaction #499707
title compound
Ausbeute 0.9%DOI: 10.6084/m9.figshare.5104873.v1
Cl.Cl.N=C(N)N1CCc2ccc(OCC3(C(=O)O)CCN(c4ccncc4)CC3)cc2C1
Reaction #499708
title compound
Ausbeute 211.6%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)C1(COc2ccc3c(c2)CN(C(=O)OCc2ccccc2)CC3)CCN(c2cc(C)nc(C)c2)CC1
Reaction #499716
title compound
Ausbeute 92.7%DOI: 10.6084/m9.figshare.5104873.v1
Cc1cc(N2CCC(COc3ccc4c(c3)CN(C(=N)N)CC4)(C(=O)O)CC2)cc(C)n1.Cl.Cl
Reaction #499717
title compound
Ausbeute 188.7%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)C1(COc2ccc3ccc(C(=N)N)cc3c2Cl)CCN(c2ccncc2)CC1.Cl.Cl
Reaction #499773
title compound
DOI: 10.6084/m9.figshare.5104873.v1
Cl.Cl.N=C(N)c1ccc2ccc(OCC3(C(=O)O)CCN(c4ccncc4)CC3)c(Cl)c2c1
Reaction #499774
title compound
Ausbeute 132.5%DOI: 10.6084/m9.figshare.5104873.v1
Cl.Cl.N=C(N)N1CCCc2ccc(OCC3(C(=O)O)CCN(c4ccncc4)CC3)cc2C1
Reaction #499778
title compound
Ausbeute 197.2%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)C1(CSc2ccc3c(c2)CN(C(C)=O)CC3)CCN(c2ccncc2)CC1
Reaction #499779
title compound
DOI: 10.6084/m9.figshare.5104873.v1
Br.Br.CCOC(=O)C1(CN)CCN(c2ccncc2)CC1
Reaction #499789
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)C1(CNS(=O)(=O)c2ccc3c(c2)CN(C(=O)C(F)(F)F)CC3)CCN(c2ccncc2)CC1
Reaction #499790
title compound
Ausbeute 48.1%DOI: 10.6084/m9.figshare.5104873.v1
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