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752721

CC(C)(C)OC(=O)N1CCC(Oc2ccc(N(Cc3ccc4ccc(C#N)cc4c3)S(C)(=O)=O)cc2)CC1
Reaction #188523
DOI: 10.1039/C8SC04228D
CCCS(=O)(=O)N(Cc1ccc2ccc(C#N)cc2c1)c1ccc(OC2CCN(C(=O)OC(C)(C)C)CC2)cc1
Reaction #189004
DOI: 10.1039/C8SC04228D
CCOC(=O)CN(CC=Cc1cccc(C#N)c1)c1ccc(OC2CCN(C(=O)OC(C)(C)C)CC2)cc1
Reaction #236370
DOI: 10.1039/C8SC04228D
CCCCS(=O)(=O)N(Cc1ccc2ccc(C#N)cc2c1)c1ccc(OC2CCN(C(=O)OC(C)(C)C)CC2)cc1
Reaction #282750
DOI: 10.1039/C8SC04228D
CCS(=O)(=O)N(Cc1ccc2ccc(C#N)cc2c1)c1ccc(OC2CCN(C(=O)OC(C)(C)C)CC2)cc1
Reaction #449697
N-[4-[(1-t-butoxycarbonyl-4-piperidyl)oxy]phenyl]-N-[(7-cyano-2-naphthyl)methyl]ethanesulfonamide
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)N1CCC(Oc2ccc(N(Cc3ccc4ccc(C#N)cc4c3)S(C)(=O)=O)cc2)CC1
Reaction #449704
N-[4-[(1-t-Butoxycarbonyl-4-piperidyl)oxy]phenyl]-N-[(7-cyano-2-naphthyl)methyl]methanesulfonamide
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)N1CCC(Oc2ccc(N(Cc3ccc4ccc(C#N)cc4c3)S(=O)(=O)Cc3ccccc3)cc2)CC1
Reaction #449705
N-[4-[(1-t-Butoxycarbonyl-4-piperidyl)oxy]phenyl]-N-[(7-cyano-2-naphthyl)methyl]benzylsulfonamide
DOI: 10.6084/m9.figshare.5104873.v1
CCCS(=O)(=O)N(Cc1ccc2ccc(C#N)cc2c1)c1ccc(OC2CCN(C(=O)OC(C)(C)C)CC2)cc1
Reaction #449706
N-[4-[(1-t-Butoxycarbonyl-4-piperidyl)oxy]phenyl]-N-[(7-cyano-2-naphthyl)methyl]propanesulfonamide
DOI: 10.6084/m9.figshare.5104873.v1
CCCCS(=O)(=O)N(Cc1ccc2ccc(C#N)cc2c1)c1ccc(OC2CCN(C(=O)OC(C)(C)C)CC2)cc1
Reaction #449707
N-[4-[(1-t-Butoxycarbonyl-4-piperidyl)oxy]phenyl]-N-[(7-cyano-2-naphthyl)methyl]butanesulfonamide
DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)C(C)S(=O)(=O)N(Cc1ccc2ccc(C#N)cc2c1)c1ccc(OC2CCN(C(=O)OC(C)(C)C)CC2)cc1
Reaction #449716
ethyl 2-[N-[4-[(1-t-butoxycarbonyl-4-piperidyl)oxy]phenyl]-N-[(7-cyano-2-naphthyl)methyl]sulfamoyl]propionate
収率 81.1%DOI: 10.6084/m9.figshare.5104873.v1
CCS(=O)(=O)N(CC=Cc1cccc(C#N)c1)c1ccc(OC2CCN(C(=O)OC(C)(C)C)CC2)cc1
Reaction #771583
DOI: 10.1039/C8SC04228D
CC(C)(C)OC(=O)N1CCC(Oc2ccc(NCCOc3cccc(C#N)c3)cc2)CC1
Reaction #834958
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)N(CC=Cc1cccc(C#N)c1)c1ccc(OC2CCN(C(=O)OC(C)(C)C)CC2)cc1
Reaction #887573
DOI: 10.1039/C8SC04228D
CC(C)(C)OC(=O)N1CCC(Oc2ccc(N(Cc3ccc4ccc(C#N)cc4c3)S(=O)(=O)Cc3ccccc3)cc2)CC1
Reaction #1045395
DOI: 10.1039/C8SC04228D
CN(CC=Cc1cccc(C#N)c1)c1ccc(OC2CCN(C(=O)OC(C)(C)C)CC2)cc1
Reaction #1045467
DOI: 10.1039/C8SC04228D
CC(C)(C)OC(=O)N1CCC(Oc2ccc(N(CC=Cc3cccc(C#N)c3)CCO)cc2)CC1
Reaction #1215703
DOI: 10.1039/C8SC04228D
CCOC(=O)C(C)N(CC=Cc1cccc(C#N)c1)c1ccc(OC2CCN(C(=O)OC(C)(C)C)CC2)cc1
Reaction #1224325
DOI: 10.1039/C8SC04228D
CCS(=O)(=O)N(CC(C)=Cc1cccc(C#N)c1)c1ccc(OC2CCN(C(=O)OC(C)(C)C)CC2)cc1
Reaction #1237181
DOI: 10.1039/C8SC04228D
CCS(=O)(=O)N(C/C(C)=C/c1cccc(C(=N)N)c1)c1ccc(OC2CCN(C(C)=N)CC2)cc1.Cl.Cl
Reaction #1355339
title compound
収率 104.1%DOI: 10.6084/m9.figshare.5104873.v1
CCS(=O)(=O)N(C/C=C/c1cccc(C#N)c1)c1ccc(OC2CCN(C(=O)OC(C)(C)C)CC2)cc1
Reaction #1355356
desired compound
収率 99.9%DOI: 10.6084/m9.figshare.5104873.v1
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