子结构搜索

646206

CCOC(=O)c1c(NC(=O)Nc2ccccc2)sc(-c2ccc([N+](=O)[O-])cc2)c1C
Reaction #51530
ethyl 4-methyl-5-(4-nitrophenyl)-2-(3-phenylureido)thiophene-3-carboxylate
收率 93.4%DOI: 10.6084/m9.figshare.5104873.v1
Cc1c(-c2ccc([N+](=O)[O-])cc2)sc2c1c(=O)n(-c1ccccc1)c(=O)n2Cc1c(F)cccc1F
Reaction #51531
1-(2,6-difluorobenzyl)-5-methyl-6-(4-nitrophenyl)-3-phenylthieno[2,3-d]pyrimidine-2,4(1H, 3H)-dione
收率 88.1%DOI: 10.6084/m9.figshare.5104873.v1
CCCCCCN(C(=O)C(C)C)c1sc(CC)cc1C(=O)OCC
Reaction #55940
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)N1CCc2c(sc3nc[nH]c(=O)c23)C1
Reaction #66790
title compound
收率 88.0%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)N1Cc2sc3nc[nH]c(=O)c3c2C1
Reaction #66799
title compound
收率 52.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)N1CCc2sc3nc[nH]c(=O)c3c2C1
Reaction #66837
title compound
收率 56.4%DOI: 10.6084/m9.figshare.5104873.v1
Cc1sc2[nH]c(=S)[nH]c(=O)c2c1C
Reaction #72656
title compound
收率 24.0%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)c1c(NC(N)=S)sc(C)c1C
Reaction #72657
title compound
收率 3.0%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)c1c(N=C=S)sc(C)c1C
Reaction #72658
title compound
收率 100.0%DOI: 10.6084/m9.figshare.5104873.v1
Cc1sc2ncnc(O)c2c1C
Reaction #76694
4-hydroxy-5,6-dimethylthieno[2,3-d]pyrimidine
DOI: 10.6084/m9.figshare.5104873.v1
Cc1c(C(=O)c2cccc(O)c2)sc(N=Nc2nc(N)c(O)cc2Br)c1C(=O)OC(C)(C)C
Reaction #95994
red solid
收率 72.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)c1cc(-c2ccccc2)sc1N=Nc1nc(N)c(O)cc1Br
Reaction #95997
material
收率 103.1%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)c1c(N)sc2c1CCOC2CN
Reaction #175907
DOI: 10.1039/C8SC04228D
COc1ccc(CN2CCc3c(sc(N)c3C(=O)OC(C)(C)C)C2CNC(=O)c2cn(Cc3ccccc3)c3ccccc23)cc1
Reaction #178482
DOI: 10.1039/C8SC04228D
Cc1ccc2c(c1)N=C(N1CCN(C)CC1)c1c(sc3ccccc13)N2
Reaction #188965
DOI: 10.1039/C8SC04228D
CC(C)c1csc(NC(=O)CCCCC(=O)O)c1C(=O)OC(C)(C)C
Reaction #195715
DOI: 10.1039/C8SC04228D
CCOC(=O)c1c(-c2cccc(Cl)c2Cl)csc1N1C(=O)c2ccccc2C1=O
Reaction #196287
DOI: 10.1039/C8SC04228D
C=CCOc1ccc(-c2c(C)sc(NC(=O)CC#N)c2C(=O)OCC)cc1
Reaction #202166
DOI: 10.1039/C8SC04228D
COC(=O)c1ccccc1NC(=O)CCCCC(=O)Nc1scc(C(C)C)c1C(=O)OC(C)(C)C
Reaction #205210
DOI: 10.1039/C8SC04228D
CC(C)(C)OC(=O)c1c(N)sc2c1CCOC2CN
Reaction #213452
DOI: 10.1039/C8SC04228D
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