参与 218 个反应

48

OC1CCN(c2ccncc2)C1
Reaction #651
收率 43.0%750 AstraZeneca ELN dataset
c1ccc(Nc2ccncc2)cc1
Reaction #667
收率 24.9%750 AstraZeneca ELN dataset
c1ccc(Nc2ccncc2)cc1
Reaction #668
收率 40.9%750 AstraZeneca ELN dataset
c1ccc(Nc2ccncc2)cc1
Reaction #669
收率 20.3%750 AstraZeneca ELN dataset
CCOC(=O)N1CCC(Nc2ccncc2)CC1
Reaction #48352
title compound
收率 41.1%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
CC(C)(C)OC(=O)N[C@@H]1CC[C@@H](c2cccc(F)c2F)CN(c2ccncc2)C1=O
Reaction #48426
title compound
收率 22.4%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
CC(C)(C)OC(=O)N1CCN(c2ccncc2)CC1
Reaction #74279
tert-Butyl 4-(pyridin-4-yl)piperazine-1-carboxylate
收率 47.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_09
COC(=O)C=Cc1ccncc1
Reaction #83278
methyl 3-(4-pyridyl)propenoate
收率 93152.5%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1997_04
O=C1C2CCC(CC2)N1c1ccncc1
Reaction #176987
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
CC(Nc1nccc(-n2cnc3cc(Nc4ccncc4)ccc32)n1)c1ccccc1
Reaction #181515
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
COc1ccc2cc(C(O)(c3ccncc3)c3cn(C(c4ccccc4)(c4ccccc4)c4ccccc4)cn3)ccc2c1
Reaction #189284
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
COc1cc[nH]c1C=C1C(=O)Nc2cccc(C#Cc3ccncc3)c21
Reaction #191941
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
O=Cc1ccc(-c2nc3ccccn3c2-c2ccncc2)cc1
Reaction #194895
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
CC1(C)COC(c2cc(-c3ccncc3)cc(C(F)(F)F)c2)=N1
Reaction #197564
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
CC(C)(C)OC(=O)Nc1ccc(-c2ccncc2)cc1[N+](=O)[O-]
Reaction #201232
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
CCC[CH2][Sn]([CH2]CCC)([CH2]CCC)[c]1ccncc1
Reaction #205833
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
Cn1nnc(-c2ccc3c(c2)c(C2=CCN(CCN4CCNC4=O)CC2)cn3-c2ccncc2)n1
Reaction #210186
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
O=C1CCCN1Nc1ccncc1
Reaction #231670
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
Fc1ccc(-c2ccn3c(-c4cccc(Nc5ccncc5)c4)cnc3c2)cc1
Reaction #232494
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
CN(C)CCn1ncc2ccc(-c3ccncc3)cc21
Reaction #243984
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
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