Substructure Search

18733

COc1ccccc1C(C)NCc1ccc(CN(Cc2nc3ccccc3[nH]2)C2CCCc3cccnc32)cc1
Reaction #7266
desired product
Yield 31.2%DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc(C(CC(=O)Nc2ccc(NC(=O)Nc3ccccc3C)cc2)NC(=O)c2ccc(C(=O)O)cc2)cc1OC
Reaction #9401
4-{[(1-(3,4-Dimethoxyphenyl)-3-{[4-({[(2-methylphenyl)amino]carbonyl}amino)phenyl]amino}-3-oxopropyl)amino]carbonyl}benzoic acid
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)c1ccc(CN(CCc2ccc(Cl)cc2)C(=O)c2cc(C(F)(F)F)cc(Cl)c2F)cc1
Reaction #48086
light yellow amorphous material
Yield 70.1%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)c1ccc(CN(CCc2cccc(O)c2)C(=O)c2cc(C(F)(F)F)cc(Cl)c2F)cc1
Reaction #48088
colorless amorphous material
Yield 80.2%DOI: 10.6084/m9.figshare.5104873.v1
CCc1cc(Cl)cc(C(=O)N(CCc2cc(F)cc(C(F)(F)F)c2)Cc2ccc(C(C)(C)C)cc2)c1
Reaction #48089
yellow solid
Yield 61.5%DOI: 10.6084/m9.figshare.5104873.v1
CCCc1cc(Cl)cc(C(=O)N(CCc2cccc(C(F)(F)F)c2)Cc2ccc(C(C)(C)C)cc2)c1
Reaction #48090
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CCCc1cc(Cl)cc(C(=O)N(CCc2cc(F)cc(C(F)(F)F)c2)Cc2ccc(C(C)(C)C)cc2)c1
Reaction #48091
N-(4-tert-butyl-benzyl)-3-chloro-N-[2-(3-fluoro-5-trifluoromethyl-phenyl)-ethyl]-5-propyl-benzamide
DOI: 10.6084/m9.figshare.5104873.v1
CCc1cc(CCN(Cc2ccc(C(C)(C)C)cc2)C(=O)c2cc(C(F)(F)F)cc(Cl)c2F)ccc1F
Reaction #48092
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CCCc1cc(CCN(Cc2ccc(C(C)(C)C)cc2)C(=O)c2cc(C(F)(F)F)cc(Cl)c2F)ccc1F
Reaction #48093
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CN(CCO[Si](C)(C)C(C)(C)C)C1(C(NC(=O)c2cccc(C(F)(F)F)c2Cl)c2ccccc2)CCCC1
Reaction #49088
title compound
Yield 99.9%DOI: 10.6084/m9.figshare.5104873.v1
CN(CCO)C1(C(NC(=O)c2cccc(C(F)(F)F)c2Cl)c2ccccc2)CCCC1
Reaction #49121
desired product
DOI: 10.6084/m9.figshare.5104873.v1
Cc1ccc(C(=O)NC(C)(C)c2ccccc2)cc1Cl
Reaction #49525
3-chloro-4-methyl-N-(1-methyl-1-phenylethyl)benzamide
Yield 97.2%DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc2cc(C(=O)O)ccc2c1CNCc1ccc(N(C)C)cc1
Reaction #51510
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)N1CCC(COCC(NC(=O)c2ccc3cc[nH]c3c2)c2ccccc2Cl)CC1
Reaction #60710
N-[1-(2-Chlorophenyl)-2-(1-isopropylpiperidin-4-ylmethoxy)-ethyl]-1H-indole-6-carboxamide
DOI: 10.6084/m9.figshare.5104873.v1
NC(=O)c1c(N)c2ccccc2[nH]c1=O
Reaction #72683
crude final product
Yield 249.5%DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc(CNc2c(C(=O)N(Cc3ccc(OC)cc3)Cc3ccc(OC)cc3)c(=O)[nH]c3ccccc23)cc1
Reaction #72684
N,N-bis(4-methoxybenzyl)-4-(4-methoxybenzylamino)-2-oxo-1,2-dihydroquinoline-3-carboxamide
Yield 71.0%DOI: 10.6084/m9.figshare.5104873.v1
Cc1csc2ncnc(NC3Cc4ccc(C(=O)NCc5ccccc5)cc4C3)c12
Reaction #76711
title compound
Yield 63.6%DOI: 10.6084/m9.figshare.5104873.v1
Cn1cncc1C(N)(c1ccc(Cl)nc1)c1ccc2c(c1)c(-c1cccc(Cl)c1)cc(=O)n2CC1CC1
Reaction #78465
title compound
DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc(CN(Cc2ccc(OC)cc2)S(=O)(=O)CCCN2CC(c3cccc(C(F)(F)F)c3)N(c3ccc(Oc4ccc(Cl)cc4)cc3)C2=O)cc1
Reaction #173932
DOI: 10.1039/C8SC04228D
COC1CN(CCn2c(=O)ccc3c(F)cc(F)cc32)CCC1N
Reaction #175098
DOI: 10.1039/C8SC04228D
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