Recherche de Sous-structure

753145

C1CCN(N2CCCCC2)CC1
Reaction #11324
piperidino-piperidine
Rendement 79.0%DOI: 10.6084/m9.figshare.5104873.v1
CC1=Nc2c(c(=O)n(C)c3nc(-c4ccc(Cl)cc4Cl)c(-c4ccc(Cl)cc4)cc23)C(C)(C)O1
Reaction #42085
9-(4-Chlorophenyl)-8-(2,4-dichlorophenyl)-2,4,4,6-tetramethyl-4,6-dihydro-5H-[1,3]oxazino[5,4-c]-1,8-naphthyridin-5-one
DOI: 10.6084/m9.figshare.5104873.v1
CCC(=O)N(CC(C)C)c1nc(-c2ccc(Cl)cc2Cl)c(-c2ccc(Cl)cc2)cc1C#N
Reaction #42101
N-(6-(2,4-dichlorophenyl)-5-(4-chlorophenyl)-3-cyanopyridin-2-yl)-N-isobutylpropionamide
DOI: 10.6084/m9.figshare.5104873.v1
CCCC(=O)N(C)c1nc(-c2ccc(Cl)cc2Cl)c(-c2ccc(Cl)cc2)cc1C#N
Reaction #42105
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)CC(=O)N(C)c1nc(-c2ccc(Cl)cc2Cl)c(-c2ccc(Cl)cc2)cc1C#N
Reaction #42107
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CCCN(C(=O)CC)c1nc(-c2ccc(Cl)cc2Cl)c(-c2ccc(Cl)cc2)cc1C#N
Reaction #42109
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)CN(C(=O)CCl)c1nc(-c2ccccc2Cl)c(-c2ccc(Cl)cc2)cc1C#N
Reaction #42114
2-chloro-N-(6-(2-chlorophenyl)-5-(4-chlorophenyl)-3-cyanopyridin-2-yl)-N-isobutylacetamide
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(O)c1cnc2nnn(Cc3ccc4ncccc4c3)c2n1
Reaction #44277
2-(3-quinolin-6-ylmethyl-3H-[1,2,3]triazolo[4,5-b]pyrazin-5-yl)-propan-2-ol
Rendement 4.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(=O)c1ccc2ncccc2c1
Reaction #44301
1-quinolin-6-yl-ethanone
Rendement 97.1%DOI: 10.6084/m9.figshare.5104873.v1
CCCC(=O)c1ccccc1
Reaction #49840
ketone
DOI: 10.6084/m9.figshare.5104873.v1
—
Reaction #51632
solid
Rendement 49.0%DOI: 10.6084/m9.figshare.5104873.v1
CN(CC(O)c1ccc(C=O)cc1)C(=O)OC(C)(C)C
Reaction #51994
product
Rendement 68.6%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)C(=O)c1ccc(O)cc1O
Reaction #57513
solid
Rendement 62.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(O)c1ccc2c(c1)CCCC2NC(=O)OC(C)(C)C
Reaction #60392
title compound
DOI: 10.6084/m9.figshare.5104873.v1
Oc1cccc2c1Sc1ccccc1S2
Reaction #62072
title compound
Rendement 36.0%DOI: 10.6084/m9.figshare.5104873.v1
CCC(Br)C(=O)c1ccsc1
Reaction #66704
2-Bromo-1-thiophen-3-yl-butan-1-one
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)Oc1ccc2c(C(=O)NCc3ccc(F)c(F)c3)c(C(C)O)n(Cc3ccccn3)c2c1
Reaction #68385
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CC(=O)c1ccc(Br)cc1Cl
Reaction #68554
1-(4-bromo-2-chlorophenyl)ethanone
DOI: 10.6084/m9.figshare.5104873.v1
CC(=O)c1ccc2ncccc2c1
Reaction #68603
1-(quinolin-6-yl)ethanone
Rendement 86.6%DOI: 10.6084/m9.figshare.5104873.v1
Cc1cc(-c2ccc3onc(C(F)(F)c4ccc5ncccc5c4)c3n2)sn1
Reaction #68616
product
Rendement 3.5%DOI: 10.6084/m9.figshare.5104873.v1
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