Busqueda de Subestructura

1272640

COc1ccccc1C1CCNCC1
Reaction #185383
DOI: 10.1039/C8SC04228D
Cc1ccc(N2CCC(C#N)C(=O)C2=O)cc1
Reaction #477182
compound
Rendimiento 51.6%DOI: 10.6084/m9.figshare.5104873.v1
Cc1ccc(N2CCc3c(N)n[nH]c3C2=O)cc1
Reaction #477183
compound
Rendimiento 86.0%DOI: 10.6084/m9.figshare.5104873.v1
O=C1c2c(c(C(F)(F)F)nn2-c2ccc(F)c(Cl)c2)CCN1c1ccc(I)cc1
Reaction #579108
1-(3-chloro-4-fluorophenyl)-6-[4-iodophenyl]-3-(trifluoromethyl)-1,4,5,6-tetrahydro-7H-pyrazolo[3,4-c]pyridin-7-one
Rendimiento 75.0%DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc(-n2nc(C(F)(F)F)c3c2C(=O)N(c2ccc(I)cc2)CC3)cc1
Reaction #584610
pyrazole
Rendimiento 74.0%DOI: 10.6084/m9.figshare.5104873.v1
O=C1c2c(c(C(F)(F)F)nn2-c2ccc(F)c(Cl)c2)CCN1c1ccc(I)cc1
Reaction #726735
1-(3-chloro-4-fluorophenyl)-6-[4-iodophenyl]-3-(trifluoromethyl)-1,4,5,6-tetrahydro-7H-pyrazolo[3,4-c]pyridin-7-one
Rendimiento 75.0%DOI: 10.6084/m9.figshare.5104873.v1
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Reaction #741780
tan needles
DOI: 10.6084/m9.figshare.5104873.v1
CC1=C(C)C(=O)C(=O)N=C1
Reaction #967199
acid ( D )
DOI: 10.6084/m9.figshare.5104873.v1
O=C1CCCNC1=O
Reaction #967215
Solvent B
DOI: 10.6084/m9.figshare.5104873.v1
O=C1c2c(c(C(F)(F)F)nn2-c2ccc(F)c(Cl)c2)CCN1c1ccc(I)cc1
Reaction #977695
1-(3-chloro-4-fluorophenyl)-6-[4-iodophenyl]-3-(trifluoromethyl)-1,4,5,6-tetrahydro-7H-pyrazolo[3,4-c]pyridine-7-one
Rendimiento 75.0%DOI: 10.6084/m9.figshare.5104873.v1
O=C1c2c(c(C(F)(F)F)nn2-c2ccc(F)c(Cl)c2)CCN1c1ccc(I)cc1
Reaction #979476
1-(3-chloro-4-fluorophenyl)-6-[4-iodophenyl]-3-(trifluoromethyl)-1,4,5,6-tetrahydro-7H-pyrazolo[3,4-c]pyridine-7-one
Rendimiento 75.0%DOI: 10.6084/m9.figshare.5104873.v1
O=C1c2c(c(C(F)(F)F)nn2-c2ccc(F)c(Cl)c2)CCN1c1ccc(I)cc1
Reaction #1151218
1-(3-chloro-4-fluorophenyl)-6-[4-iodophenyl]-3-(trifluoromethyl)-1,4,5,6-tetrahydro-7H-pyrazolo[3,4-c]pyridine-7-one
Rendimiento 75.0%DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc(-n2nc(O)c3c2C(=O)N(c2ccc([N+](=O)[O-])cc2)CC3)cc1
Reaction #1331722
3-hydroxy-1-(4-methoxy-phenyl)-6-(4-nitro-phenyl)-1,4,5,6-tetrahydro-pyrazolo[3,4-c]pyridin-7-one
DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc(-n2nc(C(F)(F)F)c3c2C(=O)N(c2ccc(C#N)cc2)CC3)cc1
Reaction #1331723
4-[1-(4-methoxy-phenyl)-7-oxo-3-trifluoromethyl-1,4,5,7-tetrahydro-pyrazolo[3,4-c]pyridin-6-yl]-benzonitrile
DOI: 10.6084/m9.figshare.5104873.v1
O=C1c2c(c(C(F)(F)F)nn2-c2ccc(F)c(Cl)c2)CCN1c1ccc(I)cc1
Reaction #1348760
1-(3-chloro-4-fluorophenyl)-6-[4-iodophenyl]-3-(trifluoromethyl)-1,4,5,6-tetrahydro-7H-pyrazolo[3,4-c]pyridin-7-one
Rendimiento 75.0%DOI: 10.6084/m9.figshare.5104873.v1
O=C1c2c(c(C(F)(F)F)nn2-c2ccc(F)c(Cl)c2)CCN1c1ccc(I)cc1
Reaction #1479104
1-(3-chloro-4-fluorophenyl)-6-[4-iodophenyl]-3-(trifluoromethyl)-1,4,5,6-tetrahydro-7H-pyrazolo[3,4-c]pyridine-7-one
Rendimiento 75.0%DOI: 10.6084/m9.figshare.5104873.v1
CN1CCCC(=O)C1=O
Reaction #1485706
title compound
Rendimiento 22.8%DOI: 10.6084/m9.figshare.5104873.v1
C#CC1(O)CCCN(C)C1=O
Reaction #1485707
title compound
Rendimiento 30.0%DOI: 10.6084/m9.figshare.5104873.v1
O=C1c2c(c(C(F)(F)F)nn2-c2ccc(F)c(Cl)c2)CCN1c1ccc(I)cc1
Reaction #1698988
1-(3-chloro-4-fluorophenyl)-6-[4-iodophenyl]-3-(trifluoromethyl)-1,4,5,6-tetrahydro-7H-pyrazolo[3,4-c]pyridine-7-one
Rendimiento 75.0%DOI: 10.6084/m9.figshare.5104873.v1
—
Reaction #1721428
title compound
DOI: 10.6084/m9.figshare.5104873.v1
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