4-amino-2-(2,6-dioxo(3-piperidyl))isoindoline-1,3-dione

O=C1CCC(N2C(=O)c3cccc(NC(=O)c4cccnc4)c3C2=O)C(=O)N1
Reaction #10057
N-[2-(2,6-dioxo(3-piperidyl))-1,3-dioxoisoindolin-4-yl]-3-pyridylcarboxamide
Ausbeute 79.3%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
O=C1CCC(N2C(=O)c3cccc(NCc4ccccc4)c3C2=O)C(=O)N1
Reaction #10059
2-(2,6-dioxo(3-piperidyl))-4-[benzylamino]isoindoline-1,3-dione
Ausbeute 16.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
O=C1CCC(N2C(=O)c3cccc(NCc4ccco4)c3C2=O)C(=O)N1
Reaction #10073
product
Ausbeute 35.4%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
COCC(=O)Nc1cccc2c1C(=O)N(C1CCC(=O)NC1=O)C2=O
Reaction #10074
product
Ausbeute 100.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
CCCCCCC(=O)Nc1cccc2c1C(=O)N(C1CCC(=O)NC1=O)C2=O
Reaction #10075
product
Ausbeute 79.1%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
CC(=O)OCC(=O)Nc1cccc2c1C(=O)N(C1CCC(=O)NC1=O)C2=O
Reaction #10076
product
Ausbeute 75.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
CCCCC(=O)Nc1cccc2c1C(=O)N(C1CCC(=O)NC1=O)C2=O
Reaction #10077
product
Ausbeute 85.3%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
COC(=O)C(=O)Nc1cccc2c1C(=O)N(C1CCC(=O)NC1=O)C2=O
Reaction #10078
product
Ausbeute 76.5%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
O=C1CCC(N2C(=O)c3cccc(NC(=O)c4ccco4)c3C2=O)C(=O)N1
Reaction #10079
product
Ausbeute 88.5%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
CCC(=O)Nc1cccc2c1C(=O)N(C1CCC(=O)NC1=O)C2=O
Reaction #10080
product
Ausbeute 88.1%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
O=C1CCC(N2C(=O)c3cccc(NC(=O)Cc4ccccc4)c3C2=O)C(=O)N1
Reaction #10081
product
Ausbeute 92.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
O=C1CCC(N2C(=O)c3cccc(NC(=O)c4ccccn4)c3C2=O)C(=O)N1
Reaction #10082
product
Ausbeute 40.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
O=C1CCC(N2C(=O)c3cccc(NC(=O)COCc4ccccc4)c3C2=O)C(=O)N1
Reaction #10090
product
Ausbeute 80.1%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
O=C1CCC(N2C(=O)c3cccc(NC(=O)COc4ccccc4)c3C2=O)C(=O)N1
Reaction #10094
product
Ausbeute 93.3%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
O=C1CCC(N2C(=O)c3cccc(NC(=O)c4cccc(F)c4)c3C2=O)C(=O)N1
Reaction #10096
product
Ausbeute 96.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
O=C1CCC(N2C(=O)c3cccc(NC(=O)c4cccc(C(F)(F)F)c4)c3C2=O)C(=O)N1
Reaction #10097
product
Ausbeute 46.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
O=C1CCC(N2C(=O)c3cccc(NC(=O)c4cccc([N+](=O)[O-])c4)c3C2=O)C(=O)N1
Reaction #10098
product
Ausbeute 95.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
CCCC(=O)Nc1cccc2c1C(=O)N(C1CCC(=O)NC1=O)C2=O
Reaction #10099
product
Ausbeute 80.1%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
CCCCCCCNc1cccc2c1C(=O)N(C1CCC(=O)NC1=O)C2=O
Reaction #10100
2-(2,6-Dioxo-piperidin-3-yl)-4-heptylamino-isoindole-1,3-dione
Ausbeute 41.1%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
O=C1CCC(N2C(=O)c3cccc(NC(=O)c4ccc(Cl)cc4)c3C2=O)C(=O)N1
Reaction #10101
4-chloro-N-[2-(2,6-dioxo-piperidin-3-yl)-1,3-dioxo-2,3-dihydro-1H-isoindol-4-yl]-benzamide
Ausbeute 81.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
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