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COC(=O)COc1ccc(C(=O)CN2CCN(c3ccncc3)CC2)cc1
Reaction #2296
title compound
DOI: 10.6084/m9.figshare.5104873.v1
O=C(O)COc1ccc(C(=O)CN2CCN(c3ccncc3)CC2)cc1
Reaction #2297
title compound
DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)COc1ccc(C(=O)C(C)N2CCN(c3ccncc3)CC2)cc1
Reaction #2301
title compound
DOI: 10.6084/m9.figshare.5104873.v1
NC(=O)COc1ccc(C(=O)CN2CCN(c3ccncc3)CC2)cc1
Reaction #2316
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CNC(=O)COc1ccc(C(=O)CN2CCN(c3ccncc3)CC2)cc1
Reaction #2317
title compound
DOI: 10.6084/m9.figshare.5104873.v1
COCCNC(=O)COc1ccc(C(=O)CN2CCN(c3ccncc3)CC2)cc1
Reaction #2318
title compound
DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)COc1ccc(OC2CCN(c3ccncc3)CC2)cc1
Reaction #2322
title compound
DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)COc1ccc(C(=O)C(C)(C)N2CCN(c3ccncc3)CC2)cc1
Reaction #2328
title compound
DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)COc1ccc(C(=O)C(C)CN2CCN(c3ccncc3)CC2)cc1
Reaction #2330
title compound
DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)COc1ccc(C(=O)C(C)N2CCN(c3ccncc3)CC2)cc1
Reaction #248694
DOI: 10.1039/C8SC04228D
O=CNc1ccc(OC2CCN(c3ccncc3)CC2)cc1
Reaction #300226
DOI: 10.1039/C8SC04228D
COC(=O)COc1ccc(C(=O)CN2CCN(c3ccncc3)CC2)cc1
Reaction #353904
title compound
DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)COc1ccc(C(=O)C(C)N2CCN(c3ccncc3)CC2)cc1
Reaction #353907
title compound
DOI: 10.6084/m9.figshare.5104873.v1
NC(=O)COc1ccc(C(=O)CN2CCN(c3ccncc3)CC2)cc1
Reaction #353924
title compound
DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)COc1ccc(OC2CCN(c3ccncc3)CC2)cc1
Reaction #353929
title compound
DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)COc1ccc(C(=O)C(C)(C)N2CCN(c3ccncc3)CC2)cc1
Reaction #353934
title compound
DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)COc1ccc(C(=O)C(C)CN2CCN(c3ccncc3)CC2)cc1
Reaction #353936
title compound
DOI: 10.6084/m9.figshare.5104873.v1
NC(=O)COc1ccc(C(=O)CN2CCN(c3ccncc3)CC2)cc1
Reaction #399329
DOI: 10.1039/C8SC04228D
CS(=O)(=O)Nc1ccc(OC2CCN(c3ccncc3)CC2)cc1
Reaction #432614
title compound
Rendimiento 62.4%DOI: 10.6084/m9.figshare.5104873.v1
Cc1ccc(S(=O)(=O)Nc2ccc(OC3CCN(c4ccncc4)CC3)cc2)cc1.Cl
Reaction #433848
N-{4-[1-(4-pyridyl)piperidin-4-yloxy]phenyl}-4-toluenesulphonamide, hydrochloride salt
Rendimiento 54.0%DOI: 10.6084/m9.figshare.5104873.v1
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