40

COC(=O)CCCc1ccc(N)cc1
Reaction #224117
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
COC(=O)CCCc1ccc(N)cc1
Reaction #285054
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (6/10)
COC(=O)CCCc1ccc(N)cc1
Reaction #752517
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (3/10)
COC(=O)CCCc1ccc(N)cc1
Reaction #972883
title compound
収率 41.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2012_08
COC(=O)CCCc1ccc(N)cc1
Reaction #1003679
40
収率 91.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2007_09
O=C(O)CCCc1ccc(NS(=O)(=O)c2ccccc2)cc1
Reaction #1003680
41
収率 96.7%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2007_09
COC(=O)CCCc1ccc(NC(=O)C2NC(CC(C)(C)C)C(C#N)(c3ccc(Cl)cc3F)C2c2cccc(Cl)c2F)cc1
Reaction #1325904
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (5/10)
COC(=O)CCCc1ccc(N)cc1
Reaction #1351530
40
収率 91.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2003_04
O=C(O)CCCc1ccc(NS(=O)(=O)c2ccccc2)cc1
Reaction #1351531
41
収率 96.7%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2003_04
COC(=O)CCCc1ccc(NC(C)(C)C#N)cc1
Reaction #1592129
compound 28
収率 96.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2015_12
CNC(=O)CCCc1ccc(N)cc1
Reaction #1592130
compound 30
収率 95.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2015_12
NC(=O)CCCc1ccc(N)cc1
Reaction #1592132
compound 33
収率 70.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2015_12
Nc1ccc(CCCC2=NCCN2)cc1
Reaction #1592136
compound 55
収率 96.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2015_12
COC(=O)CCCc1ccc(N)cc1
Reaction #1595873
methyl 4-(4-aminophenyl)butanoate
収率 28.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2015_12
COC(=O)CCCc1ccc(Nc2cc(-c3cccc(Cl)c3)nc3c2CCC3)cc1
Reaction #1595874
methyl 4-[4-[[2-(3-chlorophenyl)-6,7-dihydro-5H-cyclopenta[b]pyridin-4-yl]amino]phenyl]butanoate
収率 79.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2015_12
COC(=O)CCCc1ccc(N)cc1
Reaction #1595970
title compound
収率 96.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2015_12
NC(=O)CCCc1ccc(N)cc1
Reaction #1595971
title compound
収率 35.1%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2015_12
COC(=O)CCCc1ccc(Nc2ncnc3oc(-c4ccccc4)c(-c4ccc(OC)cc4)c23)cc1
Reaction #1645306
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (1/10)
COC(=O)CCCc1ccc(NC(=O)c2nnc(Nc3ccccc3F)o2)cc1
Reaction #1800940
title compound
収率 44.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_09
COC(=O)CCCc1ccc(N)cc1
Reaction #1894472
methyl 4-(4-aminophenyl)butanoate
収率 94.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_01
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