Busqueda de Subestructura

3928

CCOC(=O)Nc1c(F)cc(F)cc1Br
Reaction #8207
2-bromo-4,6-difluoro-N-carbethoxy aniline
Rendimiento 94.0%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)Nc1c(F)cc(F)cc1C#C[Si](C)(C)C
Reaction #8208
2-(trimethylsilylethynyl)-4,6-difluoro-N-carbethoxyaniline
Rendimiento 71.0%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)c1cc(F)c(N2CC[C@H](NC(=O)OC(C)(C)C)C2)c(F)c1NC1CC1
Reaction #10384
title compound
Rendimiento 83.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(=NNc1ccc(F)cc1F)C(=O)O
Reaction #62527
2-(2,4-difluorophenylhydrazono)propionic acid
Rendimiento 943.2%DOI: 10.6084/m9.figshare.5104873.v1
O=C(C(=C1SCS1)c1ccncc1)c1c(F)ccc(N(Cc2ccccc2)Cc2ccccc2)c1F
Reaction #66383
1-(3-dibenzylamino-2,6-difluoro-phenyl)-2-[1,3]dithietan-2-ylidene-2-pyridin-4-yl-ethanone
Rendimiento 49.0%DOI: 10.6084/m9.figshare.5104873.v1
Fc1ccc(N(Cc2ccccc2)Cc2ccccc2)c(F)c1-c1n[nH]c(S)c1-c1ccncc1
Reaction #66384
5-(3-dibenzylamino-2,6-difluoro-phenyl)-4-pyridin-4-yl-2H-pyrazole-3-thiol
DOI: 10.6084/m9.figshare.5104873.v1
Cl.Oc1cc(Nc2ncnc3sc4c(c23)CCNC4)c(F)cc1F
Reaction #66835
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CN(C)C/C=C/C(=O)N1CCc2c(sc3ncnc(Nc4cc(O)c(F)cc4F)c23)C1
Reaction #66893
5-({7-[(2E)-4-(Dimethylamino)but-2-enoyl]-5,6,7,8-tetrahydropyrido[4′,3′:4,5]thieno[2,3-d]-pyrimidin-4-yl}amino)-2,4-difluorophenol
DOI: 10.6084/m9.figshare.5104873.v1
CCn1cc(-c2ccncc2)c(-c2c(F)ccc(N)c2F)n1
Reaction #74125
desired product
Rendimiento 79.0%DOI: 10.6084/m9.figshare.5104873.v1
—
Reaction #82000
solid
Rendimiento 63.0%DOI: 10.6084/m9.figshare.5104873.v1
—
Reaction #82001
purple brown solid
Rendimiento 92.5%DOI: 10.6084/m9.figshare.5104873.v1
O=C(Nc1c([N+](=O)[O-])cc(F)c(Cl)c1F)C(F)(F)F
Reaction #82074
solid
Rendimiento 95.0%DOI: 10.6084/m9.figshare.5104873.v1
Nc1c([N+](=O)[O-])cc(F)c(Cl)c1F
Reaction #82075
crystalline yellow solid
Rendimiento 6.9%DOI: 10.6084/m9.figshare.5104873.v1
—
Reaction #82588
solid
Rendimiento 63.0%DOI: 10.6084/m9.figshare.5104873.v1
—
Reaction #82589
purple brown solid
Rendimiento 92.5%DOI: 10.6084/m9.figshare.5104873.v1
O=C(Nc1c([N+](=O)[O-])cc(F)c(Cl)c1F)C(F)(F)F
Reaction #82662
solid
Rendimiento 95.0%DOI: 10.6084/m9.figshare.5104873.v1
Nc1c([N+](=O)[O-])cc(F)c(Cl)c1F
Reaction #82663
crystalline yellow solid
Rendimiento 6.9%DOI: 10.6084/m9.figshare.5104873.v1
Nc1c(F)cc(F)c(F)c1Nc1ccc(I)cc1F
Reaction #160603
solid
Rendimiento 66.4%DOI: 10.6084/m9.figshare.5104873.v1
C=CCC1(S(=O)(=O)Nc2c(F)cc(F)c(F)c2Nc2ccc(I)cc2F)CC1
Reaction #160607
title product
DOI: 10.6084/m9.figshare.5104873.v1
Fc1ccc(-n2cnnc2-c2cc3c(s2)-c2cc(Br)ccc2OCC3)c(F)c1
Reaction #171759
293
DOI: 10.6084/m9.figshare.5104873.v1
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