Поиск подструктуры

Nc1cccc(Cl)c1

COC(=O)c1c(NC(=O)OC(C)(C)C)cc(Cl)c(OC)c1Cl
Reaction #3222
title compound
Выход 96.0%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)c1c(N)cc(Cl)c(OC)c1Cl
Reaction #3223
title compound
Выход 87.0%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)c1ccc(-n2cccc2C=O)cc1Cl
Reaction #52996
2-chloro-4-(2-formyl-1-pyrrolyl)benzoic acid methyl ester
DOI: 10.6084/m9.figshare.5104873.v1
O=c1cnn(-c2ccc(C(Cl)c3ccc(Cl)cc3Cl)c(Cl)c2)c(=O)[nH]1
Reaction #63827
2-[3-chloro-4-[chloro(2,4-dichlorophenyl)methyl]phenyl]-1,2,4-triazine-3,5(2H,4H)-dione
DOI: 10.6084/m9.figshare.5104873.v1
NC(=O)C(c1ccc(Cl)cc1)c1ccc(-n2ncc(=O)[nH]c2=O)cc1Cl
Reaction #63834
2-chloro-α-(4-chlorophenyl)-4-(4,5-dihydro-3,5-dioxo-1,2,4-triazin-2(3H)-yl)-benzeneacetamide
Выход 54.0%DOI: 10.6084/m9.figshare.5104873.v1
O=C(O)C(c1ccc(Cl)cc1)c1c(Cl)cc(-n2ncc(=O)[nH]c2=O)cc1Cl
Reaction #63835
2,6-dichloro-α-(4-chlorophenyl)-4-(4,5-dihydro-3,5-dioxo-1,2,4-triazin-2(3H)-yl)benzeneacetic acid
Выход 27.8%DOI: 10.6084/m9.figshare.5104873.v1
O=C(Cl)C(c1ccc(Cl)cc1)c1c(Cl)cc(-n2ncc(=O)[nH]c2=O)cc1Cl
Reaction #63836
2,6-dichloro-α-(4-chlorophenyl)-4-(4,5-dihydro-3,5-dioxo-1,2,4-triazin-2(3H)-yl)benzeneacetyl chloride
Выход 100.0%DOI: 10.6084/m9.figshare.5104873.v1
O=C1CNN(c2cc(Cl)c(C(C(=O)O)c3ccc(Cl)cc3)c(Cl)c2)C(=O)N1
Reaction #63843
2,6-dichloro-α-(4-chlorophenyl)-4-(3,4,5,6-tetrahydro-3,5-dioxo-1,2,4-triazin-2(1H)-yl)benzeneacetic acid
Выход 67.2%DOI: 10.6084/m9.figshare.5104873.v1
O=C(O)C1CC(c2ccccc2)c2c(Cl)cc(Cl)cc2N1
Reaction #75648
Compound 15
DOI: 10.6084/m9.figshare.5104873.v1
Cc1cccc(C2CC(C(=O)O)Nc3cc(Cl)cc(Cl)c32)c1
Reaction #75650
Compound 18
DOI: 10.6084/m9.figshare.5104873.v1
O=C(O)C1CC(c2ccc(F)cc2)c2c(Cl)cc(Cl)cc2N1
Reaction #75663
Compound 31
DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)C1CC(c2ccc(Br)cc2)c2c(Cl)cc(Cl)cc2N1
Reaction #75671
Compound 39
DOI: 10.6084/m9.figshare.5104873.v1
O=C(O)C1CC(c2ccc(Br)cc2)c2c(Cl)cc(Cl)cc2N1
Reaction #75672
Compound 40
DOI: 10.6084/m9.figshare.5104873.v1
Cc1cc(=O)n(-c2ccc(N3CCOCC3)c(Cl)c2)c(COc2ccc(Cl)c3ccccc23)n1
Reaction #84569
title compound
Выход 56.4%DOI: 10.6084/m9.figshare.5104873.v1
NCc1cc(-c2nn(-c3ccc(F)c(Cl)c3)c(=O)[nH]2)c(Cl)cc1F
Reaction #87662
desired product
Выход 42.0%DOI: 10.6084/m9.figshare.5104873.v1
Cc1ccc(-n2nc(-c3cc(CNC(=O)C(F)(F)F)c(F)cc3Cl)[nH]c2=O)cc1Cl
Reaction #87664
desired product
Выход 46.7%DOI: 10.6084/m9.figshare.5104873.v1
Cc1ccc(-n2nc(-c3cc(CNC(=O)C(F)(F)F)ccc3Cl)[nH]c2=O)cc1Cl
Reaction #87674
desired product
Выход 26.1%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)C(=O)NCc1ccc(Cl)c(-c2nn(-c3ccc(Cl)c(Cl)c3)c(=O)[nH]2)c1F
Reaction #87775
pure product
Выход 7.1%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)C(=O)NCc1cc(-c2nn(-c3ccc(F)c(Cl)c3)c(=O)[nH]2)c(Cl)cc1F
Reaction #87814
desired product
DOI: 10.6084/m9.figshare.5104873.v1
Cc1ccc(-n2nc(-c3cc(CNC(=O)C(C)(C)C)c(F)cc3Cl)[nH]c2=O)cc1Cl
Reaction #87818
desired product
DOI: 10.6084/m9.figshare.5104873.v1
Страница 1Далее