2-[3-phenyl-1-(3,4,5-trimethoxybenzoyl)pyrrolidin-3-yl]ethyl methanesulfonate

CCOCCn1c(N2CCCN(CCC3(c4ccccc4)CCN(C(=O)c4cc(OC)c(OC)c(OC)c4)C3)CC2)nc2ccccc21
Reaction #174641
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
COc1cc(C(=O)N2CCC(CCN3CCCN(c4nc5ccccc5n4CCn4cnnn4)CC3)(c3ccccc3)C2)cc(OC)c1OC
Reaction #195281
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
COc1cc(C(=O)N2CCC(CCN3CCC(Nc4nc5ccccc5n4Cc4ccc(CO)o4)CC3)(c3ccccc3)C2)cc(OC)c1OC
Reaction #210771
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
CCOCCn1c(N2CCCN(CCC3(c4ccccc4)CCN(C(=O)c4cc(OC)c(OC)c(OC)c4)C3)CC2)nc2ccccc21
Reaction #224101
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
CCOCCn1c(N2CCCN(CCC3(c4ccccc4)CCN(C(=O)c4cc(OC)c(OC)c(OC)c4)C3)CC2)nc2ccccc21
Reaction #231662
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
CCOCCn1c(N2CCCN(CCC3(c4ccccc4)CCN(C(=O)c4cc(OC)c(OC)c(OC)c4)C3)CC2)nc2ccccc21
Reaction #242895
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
COc1cc(C(=O)N2CCC(CCN3CCC(Nc4nc5ccccc5n4Cc4ccc(F)cc4)CC3)(c3ccccc3)C2)cc(OC)c1OC
Reaction #258045
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
COc1cc(C(=O)N2CCC(CCN3CCCN(c4nc5ccccc5n4CCn4ccnn4)CC3)(c3ccccc3)C2)cc(OC)c1OC
Reaction #296515
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (6/10)
CCOCCn1c(N2CCCN(CCC3(c4ccccc4)CCN(C(=O)c4cc(OC)c(OC)c(OC)c4)C3)CC2)nc2ccccc21
Reaction #386402
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (8/10)
COc1cc(C(=O)N2CCC(CCN3CCCN(c4nc5ccccc5n4CCO)CC3)(c3ccccc3)C2)cc(OC)c1OC
Reaction #393758
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (8/10)
COc1cc(C(=O)N2CCC(CCN3CCC(Nc4nc5ccccc5n4Cc4ccc(F)cc4)CC3)(c3ccccc3)C2)cc(OC)c1OC
Reaction #410393
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2001_04
COc1cc(C(=O)N2CCC(CCN3CCC(Nc4nc5ccccc5[nH]4)CC3)(c3ccccc3)C2)cc(OC)c1OC
Reaction #410425
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2001_04
COc1cc(C(=O)N2CCC(CCN3CCC(Nc4nc5ccccc5n4Cc4ccc(CO)o4)CC3)(c3ccccc3)C2)cc(OC)c1OC
Reaction #410523
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2001_04
COc1cc(C(=O)N2CCC(CCN3CCC(Nc4nc5ccccc5n4CCCC(C)=O)CC3)(c3ccccc3)C2)cc(OC)c1OC
Reaction #410529
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2001_04
CCOCCn1c(N2CCCN(CCC3(c4ccccc4)CCN(C(=O)c4cc(OC)c(OC)c(OC)c4)C3)CC2)nc2ccccc21
Reaction #724204
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2001_02
CCOCCn1c(N2CCCN(CCC3(c4ccccc4)CCN(C(=O)c4cc(OC)c(OC)c(OC)c4)C3)CC2)nc2ccccc21
Reaction #724218
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2001_02
CCOCCn1c(N2CCCN(CCC3(c4ccccc4)CCN(C(=O)c4cc(OC)c(OC)c(OC)c4)C3)CC2)nc2ccccc21
Reaction #724219
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2001_02
CCOCCn1c(N2CCCN(CCC3(c4ccccc4)CCN(C(=O)c4cc(OC)c(OC)c(OC)c4)C3)CC2)nc2ccccc21
Reaction #724220
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2001_02
CCOCCn1c(N2CCCN(CCC3(c4ccccc4)CCN(C(=O)c4cc(OC)c(OC)c(OC)c4)C3)CC2)nc2ccccc21
Reaction #724221
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2001_02
COc1cc(C(=O)N2CCC(CCN3CCCN(c4nc5ccccc5n4Cc4ccc(CO)o4)CC3)(c3ccccc3)C2)cc(OC)c1OC
Reaction #724259
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2001_02
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