Busqueda de Subestructura

197011

CNc1nc(-c2cccc(NC(=O)c3ccc(C(=O)O)c(C)c3)c2)c2cc(OC)c(OC)cc2n1.O
Reaction #69764
methyl N-[3-(6,7-dimethoxy-2-methylaminoquinazolin-4-yl)phenyl]terephthalamic acid hydrate
DOI: 10.6084/m9.figshare.5104873.v1
CNc1nc(-c2cccc(NC(=O)c3ccc(C(=O)O)c(C)c3)c2)c2cc(OC)c(OC)cc2n1.O
Reaction #69765
methyl N-[3-(6,7-dimethoxy-2-methylaminoquinazolin-4-yl)phenyl]terephthalamic acid hydrate
DOI: 10.6084/m9.figshare.5104873.v1
CNc1nc(-c2cccc(NC(=O)c3ccc(C(=O)O)c(C)c3)c2)c2cc(OC)c(OC)cc2n1.O
Reaction #69766
methyl N-[3-(6,7-dimethoxy-2-methylaminoquinazolin-4-yl)phenyl]terephthalamic acid hydrate
DOI: 10.6084/m9.figshare.5104873.v1
COc1cc2nc(Cl)nc(-c3cccc(N)c3)c2cc1OC
Reaction #69767
target product
Rendimiento 92.6%DOI: 10.6084/m9.figshare.5104873.v1
COc1cc2nc(CN)nc(-c3cccc(N)c3)c2cc1OC
Reaction #69768
target product
DOI: 10.6084/m9.figshare.5104873.v1
COc1cc2nc(Cl)nc(-c3cccc(N)c3)c2cc1OC
Reaction #69769
target product
Rendimiento 99.7%DOI: 10.6084/m9.figshare.5104873.v1
COc1cc2nc(CN)nc(-c3cccc(N)c3)c2cc1OC
Reaction #69770
target product
Rendimiento 38.7%DOI: 10.6084/m9.figshare.5104873.v1
CNc1nc(-c2cccc(NC(=O)c3ccc(C(=O)O)c(C)c3)c2)c2cc(OC)c(OC)cc2n1
Reaction #69772
crude product
DOI: 10.6084/m9.figshare.5104873.v1
CNc1nc(-c2cccc(NC(=O)c3ccc(C(=O)O)c(C)c3)c2)c2cc(OC)c(OC)cc2n1
Reaction #69773
titled compound
Rendimiento 53.2%DOI: 10.6084/m9.figshare.5104873.v1
CNc1nc(-c2cccc(NC(=O)c3ccc(C(=O)O)c(C)c3)c2)c2cc(OC)c(OC)cc2n1
Reaction #69775
crystals
Rendimiento 93.9%DOI: 10.6084/m9.figshare.5104873.v1
CNc1nc(-c2cccc(NC(=O)c3ccc(C(=O)O)c(C)c3)c2)c2cc(OC)c(OC)cc2n1.Cl
Reaction #69776
titled compound
DOI: 10.6084/m9.figshare.5104873.v1
Br.CNc1nc(-c2cccc(NC(=O)c3ccc(C(=O)O)c(C)c3)c2)c2cc(OC)c(OC)cc2n1
Reaction #69777
titled compound
DOI: 10.6084/m9.figshare.5104873.v1
CNc1nc(-c2cccc(NC(=O)c3ccc(C(=O)O)c(C)c3)c2)c2cc(OC)c(OC)cc2n1.O=S(=O)(O)O
Reaction #69778
titled compound
DOI: 10.6084/m9.figshare.5104873.v1
CNc1nc(-c2cccc(NC(=O)c3ccc(C(=O)O)c(C)c3)c2)c2cc(OC)c(OC)cc2n1.CS(=O)(=O)O
Reaction #69779
titled compound
DOI: 10.6084/m9.figshare.5104873.v1
CNc1nc(-c2cccc(NC(=O)c3ccc(C(=O)O)c(C)c3)c2)c2cc(OC)c(OC)cc2n1.Cc1ccc(S(=O)(=O)O)cc1
Reaction #69780
titled compound
Rendimiento 39.4%DOI: 10.6084/m9.figshare.5104873.v1
CNc1nc(-c2cccc(NC(=O)c3ccc(C(=O)O)c(C)c3)c2)c2cc(OC)c(OC)cc2n1.O=P(O)(O)O
Reaction #69781
titled compound
DOI: 10.6084/m9.figshare.5104873.v1
COCCOc1cc2ncnc(C3C(=O)Nc4ccc(F)cc43)c2cc1OC
Reaction #173210
DOI: 10.1039/C8SC04228D
COc1cc2c(C3C(=O)Nc4ccc(C#N)cc43)ncnc2cc1OCCn1ccnc1
Reaction #175168
DOI: 10.1039/C8SC04228D
Cl
Reaction #187947
DOI: 10.1039/C8SC04228D
Cc1ccc(C(Cl)(c2ccc3c(c2)c(-c2cccc(Cl)c2)nc2nnnn23)c2cncn2C)cc1
Reaction #189818
DOI: 10.1039/C8SC04228D
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