ethyl 5-(4-methoxyphenyl)-1,3,4-oxadiazole-2-carboxylate

COc1ccc(-c2nnc(C(=O)N3CC(Oc4ccc(CN5CCCC5)c(OC)c4C)C3)o2)cc1
Reaction #245724
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
COc1ccc(-c2nnc(C(=O)N3CC(Oc4ccc(CN(C)C)c(C)c4)C3)o2)cc1
Reaction #379020
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (8/10)
COc1ccc(-c2nnc(C(=O)N3CC(Oc4ccc(CN5CCN(C)CC5)c(Cl)c4)C3)o2)cc1
Reaction #407450
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (8/10)
COc1ccc(-c2nnc(C(=O)N3CC(Oc4ccc(CN(C)C)c(Cl)c4)C3)o2)cc1
Reaction #1024228
DOI: 10.1039/C8SC04228DValidation data from https://doi.org/10.1039/C8SC04228D
COc1ccc(-c2nnc(C(=O)N3CC(Oc4ccc(CN5CCOCC5)cc4C)C3)o2)cc1
Reaction #1048926
DOI: 10.1039/C8SC04228DValidation data from https://doi.org/10.1039/C8SC04228D
COc1ccc(-c2nnc(C(=O)N3CC(Oc4ccc(CN5CCOCC5)cc4C)C3)o2)cc1
Reaction #1122360
12
Rendimiento 71.8%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_10
COc1ccc(-c2nnc(C(=O)N3CC(Oc4ccc(CN(C)C)c(C)c4)C3)o2)cc1
Reaction #1122369
20
Rendimiento 74.6%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_10
CN1CCN(Cc2ccc(OC3CN(C(=O)c4nnc(-c5ccccc5)o4)C3)cc2F)CC1
Reaction #1122380
29
Rendimiento 32.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_10
COc1ccc(-c2nnc(C(=O)N3CC(Oc4ccc(CN5CCC5)cc4)C3)o2)cc1
Reaction #1122389
41
Rendimiento 68.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_10
COc1ccc(-c2nnc(C(=O)N3CC(Oc4ccc(CN(C)C)c(Cl)c4)C3)o2)cc1
Reaction #1122393
47
Rendimiento 82.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_10
COc1ccc(-c2nnc(C(=O)N3CC(Oc4ccc(CN5CCN(C)CC5)c(Cl)c4)C3)o2)cc1
Reaction #1122395
49
Rendimiento 64.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_10
COc1ccc(-c2nnc(C(=O)N3CC(Oc4ccc(CN5CCCC5)c(OC)c4C)C3)o2)cc1
Reaction #1122398
52
Rendimiento 37.2%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_10
COc1ccc(-c2nnc(C(=O)N3CC(Oc4ccc(C=O)cc4C)C3)o2)cc1
Reaction #1122403
54A
Rendimiento 38.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_10
COc1ccc(-c2nnc(C(=O)N3CC(Oc4ccc(C=O)cc4)C3)o2)cc1
Reaction #1122404
55A
Rendimiento 32.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_10
COc1ccc(-c2nnc(C(=O)N3CC(Sc4ccc(CN5CCCC5)cc4)C3)o2)cc1
Reaction #1122409
59
Rendimiento 24.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_10
COc1ccc(-c2nnc(C(=O)N3CC(O)C3)o2)cc1
Reaction #1122424
73A
Rendimiento 77.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_10
COc1ccc(-c2nnc(C(=O)N3CC(O)C3)o2)cc1
Reaction #1726689
4A
Rendimiento 77.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2012_02
COc1ccc(-c2nnc(C(=O)N3CC(Sc4ccc(CN5CCCC5)cc4)C3)o2)cc1
Reaction #2247474
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (4/10)
COc1ccc(-c2nnc(C(=O)N3CC(Oc4ccc(CN5CCC5)cc4)C3)o2)cc1
Reaction #2403600
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (10/10)