부분 구조 검색

759153

CCC1CN(c2ccc(Cl)c(C(F)(F)F)c2)C(c2cccc(C#N)c2)O1
Reaction #4219
2-m-Cyanophenyl-3-(3-trifluoromethyl-4-chlorophenyl)-5-ethyl oxazolidine
DOI: 10.6084/m9.figshare.5104873.v1
CN1CCN=C1c1ccc(C(=O)Nc2ccc(Cl)cc2C(=O)Nc2ccc(Cl)cn2)cc1
Reaction #40403
N-{4-chloro-2-[N-(5-chloro(2-pyridyl))carbamoyl]phenyl}[4-(1-methyl(2-imidazolin-2-yl))phenyl]carboxamide
DOI: 10.6084/m9.figshare.5104873.v1
CN1CCN=C1c1ccc(C(=O)Nc2ccc(Cl)cc2C(=O)Nc2ccc(Cl)cn2)cc1
Reaction #40430
N-{4-chloro-2-[N-(5-chloro(2-pyridyl))carbamoyl]phenyl}[4-(1-methyl(2-imidazolin-2-yl))phenyl]carboxamide
DOI: 10.6084/m9.figshare.5104873.v1
N=C(N)C1=NN(c2ccc(Cl)cc2)C(c2ccccc2)C1
Reaction #48037
1-(4-chlorophenyl)-5-phenyl-4,5-dihydro-(1H)-pyrazole-3-carboxamidine
DOI: 10.6084/m9.figshare.5104873.v1
N=C(NS(=O)(=O)c1ccc(F)cc1)C1=NN(c2ccc(Cl)cc2)C(c2ccccc2)C1
Reaction #48038
N-[(4-fluorophenyl)sulfonyl]-1-(4-chlorophenyl)-5-phenyl-4,5-dihydro-(1H)-pyrazole-3-carboxamidine
수율 54.0%DOI: 10.6084/m9.figshare.5104873.v1
CN=C(NS(=O)(=O)N1CCCCC1)C1=NN(c2ccc(Cl)cc2)C(c2ccccc2)C1
Reaction #48040
N-[(piperidin-1-yl)sulfonyl]-N′-methyl-1-(4-chlorophenyl)-5-phenyl-4,5-dihydro-(1H)-pyrazole-3-carboxamidine
수율 49.0%DOI: 10.6084/m9.figshare.5104873.v1
O=C1Nc2ccc([N+](=O)[O-])cc2/C1=C(/Nc1ccc(Cl)cc1)c1ccccc1
Reaction #53076
(Z)-3-[1-(4-chlorophenylamino)-1-phenyl-methylidene]-5-nitro-2-indolinone
DOI: 10.6084/m9.figshare.5104873.v1
N#CC1c2ccccc2C(Nc2ccc(Cl)cc2)=NN1C(=O)c1ccccc1
Reaction #78190
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CC(Nc1nccc(-n2cnc3ccccc32)n1)c1cccc(C(=O)Nc2ccc(Cl)cc2)c1
Reaction #174033
DOI: 10.1039/C8SC04228D
CC(=O)N1CCN(c2cccc(C3Nc4c(cc(Cl)cc4C(=O)O)CC3(C)C)c2)CC1
Reaction #176142
DOI: 10.1039/C8SC04228D
CC(=O)N(c1ccc(Cl)cc1)C1CC(C)N(C(=O)c2ccc(CCC(=O)O)cc2)c2ccccc21
Reaction #178144
DOI: 10.1039/C8SC04228D
CC(=O)N(c1ccc(Cl)cc1)C1CC(C)N(C(=O)c2ccc(OCCn3ccnc3)cc2)c2ccccc21
Reaction #179692
DOI: 10.1039/C8SC04228D
CC(=O)N(c1ccc(Cl)cc1)C1CC(C)N(C(=O)c2cccc(C(=O)O)c2)c2ccccc21
Reaction #186188
DOI: 10.1039/C8SC04228D
CCN1CCN(CC(=O)Nc2nc3ccc(Oc4cc(NC(=O)c5cccc(C(C)(C)C#N)c5)c(F)cc4Cl)nc3s2)CC1
Reaction #187824
DOI: 10.1039/C8SC04228D
CCOC(=O)COc1ccc2c(c1)N(C(=O)c1ccc(N(C)C)cc1)C(C)CC2N(C(C)=O)c1ccc(Cl)cc1
Reaction #188086
DOI: 10.1039/C8SC04228D
CCC(=O)N(c1ccc(Cl)cc1)C1CC(C)N(C(=O)c2ccc(F)cc2)c2ccc(C=CC(=O)O)cc21
Reaction #191123
DOI: 10.1039/C8SC04228D
Cc1cc(N(Cc2ccccc2)C(=O)C2CCN(C(=O)OC(C)(C)C)CC2)c(Br)cc1Cl
Reaction #192108
DOI: 10.1039/C8SC04228D
N=C(c1ccc(C(=O)Nc2ccc(Cl)c(-c3ccccn3)c2)cc1)N1CCOCC1
Reaction #204251
DOI: 10.1039/C8SC04228D
Cc1ccc(-c2nnn(CC3OC(=O)N(c4ccc(Cl)cc4)C3c3cc(F)cc(F)c3)n2)cn1
Reaction #208566
DOI: 10.1039/C8SC04228D
CN1CCN(C(=N)c2ccc(C(=O)Nc3ccc(Cl)c(-c4ccccn4)c3)cc2)CC1
Reaction #211248
DOI: 10.1039/C8SC04228D
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