Участвует в 610 реакциях

52

NS(=O)(=O)c1cccc(Nc2cncnc2)c1
Reaction #547
Выход 18.8%750 AstraZeneca ELN dataset
c1ncc(C23CCCN2CCC3)cn1
Reaction #3388
oil
Выход 18.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
O=C(c1cncnc1)c1ccc(Cl)cc1Cl
Reaction #4607
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1988_02
CC(C)N1CCC(Oc2ccc3c(c2)cc(C(=O)N2CCC(F)(F)CC2)n3-c2cncnc2)CC1
Reaction #48153
desired product
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
Oc1ccc(Oc2cncnc2)cc1
Reaction #163312
5-(4-Hydroxy-phenoxy)-pyrimidine
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_09
CC(C)(C)OC(=O)N1CC2CC1CN2c1cncnc1
Reaction #186958
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
[CH3][Sn]([CH3])([CH3])[c]1cncnc1
Reaction #194829
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
CC(C)(C)OC(=O)N1CCCC1C#Cc1cncnc1
Reaction #200319
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
Cc1c(NC(=O)CC(C)(C)C)c(C)c2c(c1-c1cncnc1)OCC2c1ccc(C(C)C)cc1
Reaction #213336
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
CCOCc1nc2c(c(C)c(C)n3nnnc23)n1CCOCC#Cc1cncnc1
Reaction #223722
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
COc1ccc(CNc2cncnc2)cc1
Reaction #229836
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
CC(c1ccc(-c2cncnc2)cc1)N1CCC(CCCO)(c2ccc(F)cc2)OC1=O
Reaction #235447
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
CC(C)(C)OC(=O)N1CCC(Nc2cncnc2)CC1
Reaction #240394
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
Clc1ccc(Nc2nnc(-c3ccc(Oc4cncnc4)cc3)o2)cc1
Reaction #241144
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
c1ccc(C2CCCCC2N2CCC(Nc3cncnc3)CC2)cc1
Reaction #244075
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
CCOC(=O)C=Cc1cncnc1
Reaction #245067
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
CC(C)N1CCC(Oc2ccc3c(c2)cc(C(=O)N2CCC(F)(F)CC2)n3-c2cncnc2)CC1
Reaction #248809
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
COCCn1ccc(NC(=O)c2nc(C)ccc2Nc2cncnc2)n1
Reaction #254697
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
CC(c1ccc(-c2cncnc2)cc1Cl)C(O)(c1ccc2oc(=O)n(C)c2c1)C(F)(F)F
Reaction #265701
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (6/10)
FC(F)(F)c1cccc(Nc2nnc(-c3ccc(Oc4cncnc4)cc3)o2)c1
Reaction #268243
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (6/10)
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