子结构搜索

6266

Cc1ccc(-c2c(N)ncnc2Cl)cc1
Reaction #2400
6-chloro-5-(4-methylphenyl)pyrimidin-4-amine
DOI: 10.6084/m9.figshare.5104873.v1
Cc1ccc(-c2c(N)ncnc2OCCO)cc1
Reaction #2401
2-{6-amino-5-(4-methylphenyl)pyrimidin-4-yloxy}-ethanol
DOI: 10.6084/m9.figshare.5104873.v1
Cc1ccc(-c2c(Cl)ncnc2NS(=O)(=O)CCc2ccccc2)cc1
Reaction #8689
2-phenyl-ethanesulfonic acid (6-chloro-5-p-tolyl-pyrimidin-4-yl)-amide
收率 59.6%DOI: 10.6084/m9.figshare.5104873.v1
Cc1ccc(-c2c(NS(=O)(=O)CCc3ccccc3)ncnc2OCCO)cc1
Reaction #8690
2-phenyl-ethanesulfonic acid [6-(2-hydroxy-ethoxy)-5-p-tolyl-pyrimidin-4-yl]-amide
DOI: 10.6084/m9.figshare.5104873.v1
Cc1ccc(-c2c(Cl)nc(-c3ccncc3)nc2NS(=O)(=O)CCc2ccccc2)cc1
Reaction #8692
2-phenyl-ethanesulfonic acid (6-chloro-2-pyridin-4-yl-5-p-tolyl-pyrimidin-4-yl)-amide
收率 21.8%DOI: 10.6084/m9.figshare.5104873.v1
Cc1ccc(-c2c(NS(=O)(=O)CCc3ccccc3)nc(-c3ccncc3)nc2OCCO)cc1
Reaction #8693
2-phenyl-ethanesulfonic acid [6-(2-hydroxy-ethoxy)-2-pyridin-4-yl-5-p-tolyl-pyrimidin-4-yl]-amide
DOI: 10.6084/m9.figshare.5104873.v1
Cc1ccc(-c2c(NS(=O)(=O)CCc3ccccc3)ncnc2OCCOc2ccc(Br)cc2)cc1
Reaction #8714
2-phenyl-ethanesulfonic acid {6-[2-(4-bromo-phenoxy)-ethoxy]-5-p-tolyl-pyrimidin-4-yl}-amide
收率 86.7%DOI: 10.6084/m9.figshare.5104873.v1
Cc1ccc(NS(=O)(=O)Nc2ncnc(Cl)c2-c2ccc(C)cc2)cc1
Reaction #10342
4-methyl-phenyl sulfamic acid-[6-chloro-5-(p-tolyl)-4-pyrimidinyl]-amide
收率 62.1%DOI: 10.6084/m9.figshare.5104873.v1
Cc1ccc(NS(=O)(=O)Nc2ncnc(OCCO)c2-c2ccc(C)cc2)cc1
Reaction #10352
4-methyl-phenyl sulfamic acid-[6-(2-hydroxy-ethoxy)-5-(p-tolyl)-4-pyrimidinyl]-amide
DOI: 10.6084/m9.figshare.5104873.v1
CC(=O)OCC(C)(C)c1ccc(S(=O)(=O)Nc2ncnc(Cl)c2-c2ccc(C)cc2)cc1
Reaction #213644
DOI: 10.1039/C8SC04228D
Cc1ccc(-c2c(N)ncnc2OCCO)cc1
Reaction #223322
DOI: 10.1039/C8SC04228D
CCS(=O)(=O)Nc1ncnc(Cl)c1-c1ccc(C)cc1
Reaction #240579
DOI: 10.1039/C8SC04228D
CCCS(=O)(=O)Nc1ncnc(OCCO)c1-c1ccc(C)cc1
Reaction #249943
DOI: 10.1039/C8SC04228D
CCS(=O)(=O)N(C)CCOc1ncnc(NS(=O)(=O)c2ccc(C(C)(C)C)cc2)c1-c1ccc(C)cc1
Reaction #260842
DOI: 10.1039/C8SC04228D
CCS(=O)(=O)Nc1ncnc(OCCO)c1-c1ccc(C)cc1
Reaction #261600
DOI: 10.1039/C8SC04228D
COCC#CCOc1ncnc(NS(=O)(=O)c2ccc(C(C)(C)C)cc2)c1-c1ccc(C)cc1
Reaction #278720
DOI: 10.1039/C8SC04228D
COC(=O)c1cnn2c(NC(C)C(C)C)c(-c3ccc(C#N)cc3Cl)c(Cl)nc12
Reaction #295864
DOI: 10.1039/C8SC04228D
Cc1ccc(-c2c(Cl)nc3ncnn3c2NC2CCCC2)cc1
Reaction #320757
5-chloro-6-(4-methylphenyl)-7-cyclopentylamino-1,2,4-triazolo[1,5-a]pyrimidine
收率 87.0%DOI: 10.6084/m9.figshare.5104873.v1
Cc1ccc(-c2c(N)ncnc2OCCO)cc1
Reaction #392141
DOI: 10.1039/C8SC04228D
Cc1ccc(-c2c(NS(=O)(=O)c3ccc(C(C)(C)COC4CCCCO4)cc3)ncnc2OCCO)cc1
Reaction #408570
DOI: 10.1039/C8SC04228D
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