子结构搜索

4207

CCOc1cc(Oc2cccc(C(F)(F)F)c2)nc(SC)n1
Reaction #897
4-ethoxy-2-methylthio-6-[3-(trifluoromethyl)phenoxy]pyrimidine
DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc(CSc2nc(Cl)cc(Nc3cc(C)n[nH]3)n2)cc1
Reaction #7709
[6-chloro-2-(4-methoxy-benzylsulfanyl)-pyrimidin-4-yl)-(5-methyl-2H-pyrazol-3-yl)-amine
DOI: 10.6084/m9.figshare.5104873.v1
CSc1nc(Cl)cc(Nc2cc(C)n[nH]2)n1
Reaction #7714
[6-chloro-2-methylsulfanyl-pyrimidin-4-yl)-(5-methyl-2H-pyrazol-3-yl)-amine
DOI: 10.6084/m9.figshare.5104873.v1
COc1ccccc1Oc1c(Cl)nc(SC)nc1NS(=O)(=O)NCc1ccccc1
Reaction #10355
benzylsulfamic acid [6-chloro-5-(2-methoxy-phenoxy)-2-methylsulfanyl-pyrimidin-4-yl]-amide
收率 79.2%DOI: 10.6084/m9.figshare.5104873.v1
CSc1nc(Cl)c(C=O)c(Nc2c(F)cccc2F)n1
Reaction #58356
4-chloro-6-(2,6-difluoro-phenylamino)-2-methylsulfanyl-pyrimidine-5-carbaldehyde
收率 76.2%DOI: 10.6084/m9.figshare.5104873.v1
CSc1nc(Cl)c(N)c(Cl)n1
Reaction #88462
solid
收率 87.0%DOI: 10.6084/m9.figshare.5104873.v1
CCOc1nc(SC)nc2sc(Cc3c(Cl)cccc3Cl)nc12
Reaction #88467
2-(2,6-dichloro-benzyl)-7-ethoxy-5-methylsulfanyl-thiazolo[5,4-d]pyrimidine
收率 41.0%DOI: 10.6084/m9.figshare.5104873.v1
C#CCNc1cc(Cl)nc(SC)n1
Reaction #91883
light yellow solid
收率 99.4%DOI: 10.6084/m9.figshare.5104873.v1
CSc1nc(Cl)c(-c2ccccc2)c(NN)n1
Reaction #93392
4-chloro-6-hydrazino-2-methylthio-5-phenylpyrimidine
DOI: 10.6084/m9.figshare.5104873.v1
CSc1nc(Cl)c(C#N)c(N[C@@H](C)c2nc3ccn(C)c3cc2-c2ccnn2C)n1
Reaction #162461
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CSc1nc(Cl)c(C#N)c(N[C@@H](C)c2nc3ccn(C)c3cc2N2CCOCC2)n1
Reaction #162469
title compound
收率 59.0%DOI: 10.6084/m9.figshare.5104873.v1
CSc1nc(N)c(C#N)c(N[C@@H](C)c2nc3ccn(C)c3cc2N2CCOCC2)n1
Reaction #162470
title compound
收率 61.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(Oc1cc(Cl)nc(SCc2cccc(F)c2F)n1)C1COC(C)(C)O1
Reaction #176368
DOI: 10.1039/C8SC04228D
CSc1nc(Cl)c([N+](=O)[O-])c(Oc2cccc(C(=O)N(C)C)c2)n1
Reaction #179460
DOI: 10.1039/C8SC04228D
CSc1nc(Cl)c([N+](=O)[O-])c(Oc2cc(C#N)ccc2OCc2ccccc2)n1
Reaction #188923
DOI: 10.1039/C8SC04228D
Nc1nc(SCc2ccccc2)nc(Cl)c1[N+](=O)[O-]
Reaction #190313
DOI: 10.1039/C8SC04228D
CSc1nc(Cl)cc(N2CCN(C(=O)OC(C)(C)C)CC2)n1
Reaction #190489
DOI: 10.1039/C8SC04228D
CCCSc1nc(Cl)c(N)c(Cl)n1
Reaction #193318
DOI: 10.1039/C8SC04228D
CSc1nc(Cl)c([N+](=O)[O-])c(Oc2cc(C#N)ccc2OCc2ccccc2)n1
Reaction #203318
DOI: 10.1039/C8SC04228D
CSc1nc(Cl)c(C=O)c(Nc2c(F)cccc2F)n1
Reaction #209275
DOI: 10.1039/C8SC04228D
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