部分構造検索

14173

O=[N+]([O-])c1ccc(Nc2nc(Cl)nc3nc[nH]c23)cc1
Reaction #10014
2-Chloro-6-(4-nitro-phenyl-amino)-purine
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)n1cnc2c(Nc3ccc([N+](=O)[O-])cc3)nc(Cl)nc21
Reaction #10015
2-Chloro-9-isopropyl-6-(4-nitro-phenyl-amino)-9H-purine
DOI: 10.6084/m9.figshare.5104873.v1
Cn1cnc2c(Nc3ccc([N+](=O)[O-])cc3)nc(Cl)nc21
Reaction #611686
(2-Chloro-9-methyl-9H-purin-6-yl)-(4-nitro-phenyl)-amine
DOI: 10.6084/m9.figshare.5104873.v1
O=[N+]([O-])c1ccc(Nc2nc(Cl)nc3nc[nH]c23)cc1
Reaction #777487
DOI: 10.1039/C8SC04228D
CC(C)n1cnc2c(Nc3ccc([N+](=O)[O-])cc3)nc(Cl)nc21
Reaction #912976
DOI: 10.1039/C8SC04228D
Cn1cnc2c(Nc3ccc([N+](=O)[O-])cc3)nc(NN)nc21
Reaction #1025487
DOI: 10.1039/C8SC04228D
NC1CCC(Nc2nc(N3CCc4cc([N+](=O)[O-])ccc43)c3nc[nH]c3n2)CC1
Reaction #1232308
DOI: 10.1039/C8SC04228D
O=[N+]([O-])c1ccc2c(c1)CCN2c1nc(Cl)nc2[nH]cnc12
Reaction #1296018
DOI: 10.1039/C8SC04228D
Cl.Cl.N[C@H]1CC[C@H](Nc2nc(Nc3ccc([N+](=O)[O-])cc3)c3ncn(C4CCCC4)c3n2)CC1
Reaction #1332131
trans-N2-(4-aminocyclohexyl)-9-cyclopentyl-N6-(4-nitrophenyl)-9H-purin-2,6-diamine dihydrochloride
DOI: 10.6084/m9.figshare.5104873.v1
Cl.Cl.N[C@H]1CC[C@H](Nc2nc(Nc3ccc([N+](=O)[O-])cc3)c3ncn(C4CCCC4)c3n2)CC1
Reaction #1359849
trans-N2-(4-aminocyclohexyl)-9-cyclopentyl-N6-(4-nitrophenyl)-9H-purin-2,6-diamine dihydrochloride
DOI: 10.6084/m9.figshare.5104873.v1
O=[N+]([O-])c1ccc2c(c1)CCN2c1nc(Cl)nc2[nH]cnc12
Reaction #1540789
expected product
収率 90.6%DOI: 10.6084/m9.figshare.5104873.v1
N[C@H]1CC[C@H](Nc2nc(N3CCc4cc([N+](=O)[O-])ccc43)c3nc[nH]c3n2)CC1
Reaction #1540790
trans-N-[6-(2,3-dihydro-5-nitro-1H-indol-1-yl)-9H-purin-2-yl]-1,4-cyclohexanediamine
DOI: 10.6084/m9.figshare.5104873.v1
Cn1cnc2c(Nc3ccc([N+](=O)[O-])cc3)nc(Cl)nc21
Reaction #1896408
(2-Chloro-9-methyl-9H-purin-6-yl)-(4-nitro-phenyl)-amine
DOI: 10.6084/m9.figshare.5104873.v1
Cn1cnc2c(Nc3ccc([N+](=O)[O-])cc3)nc(NN)nc21
Reaction #1896432
(2-Hydrazino-9-methyl-9H-purin-6-yl)-(4-nitro-phenyl)-amine
DOI: 10.6084/m9.figshare.5104873.v1