Busqueda de Subestructura

643

Cc1ccc(-c2ncc[nH]2)cc1NC(=O)c1ccc(OCc2ncccc2N2CCN(C)CC2)cc1
Reaction #693
Rendimiento 0.0%
COc1ccc(C(=NN)Nc2ccc([N+](=O)[O-])cc2)cc1
Reaction #4693
4-methoxy-N-(4-nitrophenyl)-benzene-carbohydrazonamide
DOI: 10.6084/m9.figshare.5104873.v1
CCNC(=O)NCCCOc1cc(I)c2c(c1Cl)CNC2=O
Reaction #49607
4-chloro-5-[3-(ethylcarbamoylamino)propoxy]-7-iodoisoindolinone
Rendimiento 93.0%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)c1ccc2c(CNCc3ccc(OC(F)(F)F)cc3)c(OC)ccc2c1
Reaction #51506
product
Rendimiento 42.0%DOI: 10.6084/m9.figshare.5104873.v1
O=C(O)COc1ccc2cc(C(=O)O)ccc2c1CNCc1ccc(OC(F)(F)F)cc1
Reaction #51512
title compound
DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc(C2NC(=O)NC2=O)cc1OC1CC2CCC1C2
Reaction #64748
hydantoin
Rendimiento 71.0%DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc(CN(C)c2ccc(OC)c3nc(NC(=O)c4ccc(F)cc4)sc23)cc1
Reaction #80162
4-Fluoro-N-{4-methoxy-7-[(4-methoxy-benzyl)-methyl-amino]-benzothiazol-2-yl}-benzamide
DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc(CN(C)c2ccc(OC)c3nc(NC(=O)c4ccnc(Br)c4)sc23)cc1
Reaction #80163
2-Bromo-N-{4-methoxy-7-[(4-methoxy-benzyl)-methyl-amino]-benzothiazol-2-yl}-isonicotinamide
DOI: 10.6084/m9.figshare.5104873.v1
COc1cc(Cl)c(C(N)=O)cc1CNC(=O)C(F)(F)F
Reaction #87648
desired product
DOI: 10.6084/m9.figshare.5104873.v1
COc1cc(Cl)c(C(=O)N=C=O)cc1CNC(=O)C(F)(F)F
Reaction #87649
desired product
DOI: 10.6084/m9.figshare.5104873.v1
COc1cc(Cl)c(-c2nn(-c3ccc(C(F)(F)F)cc3)c(=O)[nH]2)cc1CNC(=O)C(F)(F)F
Reaction #87650
desired product
Rendimiento 24.5%DOI: 10.6084/m9.figshare.5104873.v1
O=C(O)c1ccc(NC(=O)c2cc(Cl)c(OC3CCCC3)c(OC3CCCC3)c2)cc1
Reaction #91010
4-(3-Chloro-4,5-bis(cyclopentyloxy)benzamido)benzoic acid
Rendimiento 77.4%DOI: 10.6084/m9.figshare.5104873.v1
Cc1nc(NCc2ccc(OC(F)(F)F)cc2)nc(NC2CCCCC2)c1C
Reaction #91379
titled compound
DOI: 10.6084/m9.figshare.5104873.v1
CC(C#N)(Cn1nc2cc(Cl)cc(CO)c2n1)NC(=O)c1ccc(OC(F)(F)F)cc1
Reaction #158146
title compound
Rendimiento 67.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(C#N)(Cn1nc2cc(Cl)cc(-c3ccc(C(F)(F)F)cc3)c2n1)NC(=O)c1ccc(OC(F)(F)F)cc1
Reaction #158151
title compound
DOI: 10.6084/m9.figshare.5104873.v1
—
Reaction #158154
solid
Rendimiento 87.0%DOI: 10.6084/m9.figshare.5104873.v1
O=c1ccc2cc(Oc3ccc(NCc4ccc(OC(F)(F)F)cc4)nn3)ccc2[nH]1
Reaction #164657
6-((6-((4-(trifluoromethoxy)benzyl)amino)pyridazin-3-yl)oxy)quinolin-2(1H)-one
Rendimiento 8.0%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)c1csc(NC(=O)c2cc(OC)c(OC)cc2O)n1
Reaction #165884
same compound ( 5a )
Rendimiento 55.2%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)c1csc(NC(=O)c2cc(OC)c(OC)cc2O)n1
Reaction #165885
title compound ( 5a )
Rendimiento 84.9%DOI: 10.6084/m9.figshare.5104873.v1
O=C1COc2ccc(CNC3CCC(C(=O)c4nc5ccccc5s4)CC3)cc2N1
Reaction #173029
DOI: 10.1039/C8SC04228D
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