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81406

Cc1ccccc1C(CCN1CCCCC1)NC(=O)Cc1ccc2ccccc2n1
Reaction #63281
subject compound
Ausbeute 95.0%DOI: 10.6084/m9.figshare.5104873.v1
Cc1ccccc1C(CCN1CCCCC1)NC(=O)Cc1ccc2ccccc2n1.O=C(O)/C=C/C(=O)O
Reaction #63282
subject compound
Ausbeute 74.0%DOI: 10.6084/m9.figshare.5104873.v1
Cc1cc(Cl)nc2nc(N3C(=O)c4ccccc4C3CC(=O)N3CCC(=O)CC3)ccc12
Reaction #173479
DOI: 10.1039/C8SC04228D
Cc1ccccc1C(CCN1CCCCC1)NC(=O)Cc1ccc2ccccc2n1
Reaction #173695
DOI: 10.1039/C8SC04228D
Cc1cc(Cl)nc2nc(N3C(=O)c4ccccc4C3CC(=O)N3CCC4(CC3)OCCO4)ccc12
Reaction #245642
DOI: 10.1039/C8SC04228D
O=C(CC1c2ccccc2C(=O)N1c1ccc(Cl)cn1)N1CCCCC1
Reaction #263180
DOI: 10.1039/C8SC04228D
O=C(CC1c2ccccc2C(=O)N1c1ccc2ccc(Cl)nc2n1)N1CCC2(CC1)OCCO2
Reaction #294759
DOI: 10.1039/C8SC04228D
O=C(CC1c2ccccc2C(=O)N1c1ccc(Cl)cn1)N1CCCCC1
Reaction #367717
colorless crystals
Ausbeute 26.2%DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc(N2C(=O)c3ccccc3C2CC(=O)N2CCCCC2)cc1
Reaction #367719
(-)-2-(4-Methoxyphenyl)-3-piperidinocarbonylmethylisoindolin-1-one
DOI: 10.6084/m9.figshare.5104873.v1
O=C(CC1c2ccccc2C(=O)N1C1CCCCC1)N1CCCCC1
Reaction #367720
2-cyclohexyl-3-piperidinocarbonylmethylisoindolin-1-one
Ausbeute 73.6%DOI: 10.6084/m9.figshare.5104873.v1
O=C(CC1c2ccccc2C(=O)N1c1ccc2ccc(Cl)nc2n1)N1CCC2(CC1)OCCO2
Reaction #891437
DOI: 10.1039/C8SC04228D
COc1ccc(N2C(=O)c3ccc(Cl)cc3C2CC(=O)N2CCC3(CC2)OCCO3)cc1
Reaction #955433
colorless crystals
Ausbeute 90.3%DOI: 10.6084/m9.figshare.5104873.v1
O=C(CC1c2ccccc2C(=O)N1c1ccc2ccc(Cl)nc2n1)N1CCC2(CC1)OCCO2
Reaction #955434
colorless crystals
Ausbeute 98.1%DOI: 10.6084/m9.figshare.5104873.v1
Cc1cc(Cl)nc2nc(N3C(=O)c4ccccc4C3CC(=O)N3CCC4(CC3)OCCO4)ccc12
Reaction #955435
colorless crystals
Ausbeute 90.2%DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc(N2C(=O)c3ccc(Cl)cc3C2CC(=O)N2CCC3(CC2)OCCO3)cc1
Reaction #1319244
DOI: 10.1039/C8SC04228D
O=C(CC1c2ccccc2C(=O)N1c1ccc(Cl)cn1)N1CCCCC1
Reaction #1725518
colorless crystals
Ausbeute 26.2%DOI: 10.6084/m9.figshare.5104873.v1
O=C(CC1c2ccccc2C(=O)N1C1CCCCC1)N1CCCCC1
Reaction #1725520
2-cyclohexyl-3-piperidinocarbonylmethylisoindolin-1-one
Ausbeute 73.6%DOI: 10.6084/m9.figshare.5104873.v1
O=C(CC1c2ccccc2-c2ccccc2N1S(=O)(=O)c1ccc(Cl)c(Cl)c1)N1CCC(Cc2ccc(C3=NCCN3)cc2)CC1
Reaction #1750428
title compound
DOI: 10.6084/m9.figshare.5104873.v1
O=C(CC1c2ccccc2-c2ccccc2N1S(=O)(=O)c1ccc(Cl)c(Cl)c1)N1CCC(Cc2ccc(C3=NCCCN3)cc2)CC1
Reaction #1750429
title compound
DOI: 10.6084/m9.figshare.5104873.v1
O=C(CC1c2ccccc2C(=O)N1c1ccc(Cl)cn1)N1CCCCC1
Reaction #2319461
colorless crystals
Ausbeute 26.2%DOI: 10.6084/m9.figshare.5104873.v1
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