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1270132

O=C1NCCC[C@H]1Nc1ncccc1Cl
Reaction #688
Ausbeute 2.0%
CN1CC(Nc2ncccc2Cl)CCC1=O
Reaction #722
Ausbeute 0.0%
CC1(N2C(=O)c3cccc(NCc4cccc(Cl)c4)c3C2=O)CCC(=O)NC1=O
Reaction #10148
product
Ausbeute 41.0%DOI: 10.6084/m9.figshare.5104873.v1
CC1(C)CCC(=O)NC1=O
Reaction #42857
3,3-dimethylpiperidin-2,6-dione
Ausbeute 86.2%DOI: 10.6084/m9.figshare.5104873.v1
CC1(C)CC(C)(C)C(=O)NC1=O
Reaction #42858
3,3,5,5-tetramethylpiperidin-2,6-dione
Ausbeute 98.4%DOI: 10.6084/m9.figshare.5104873.v1
COc1cc(/C=C2\CCCN([C@@H](C)c3ccc(F)cc3)C2=O)ccc1-n1cc(C)[n+](COP(=O)([O-])O)c1
Reaction #44597
title compound
Ausbeute 90.7%DOI: 10.6084/m9.figshare.5104873.v1
CN(C)C1CCNCC1.Cl.Cl
Reaction #51231
4-(dimethylamino)piperidine.dihydrochloride
DOI: 10.6084/m9.figshare.5104873.v1
CC1(N2C(=O)c3cscc3C2=O)CCC(=O)NC1=O
Reaction #66780
solid
Ausbeute 79.1%DOI: 10.6084/m9.figshare.5104873.v1
O=C1N(Cc2cccc3ccccc23)CCCC12CCN(c1cnc3ccccc3n1)CC2
Reaction #69820
title compound
Ausbeute 68.7%DOI: 10.6084/m9.figshare.5104873.v1
Cc1ccc(S(=O)(=O)n2cc(CN3CCCC4(CCN(C(=O)OC(C)(C)C)CC4)C3=O)c3ccccc32)cc1
Reaction #69850
tert-butyl 1-oxo-2-((1-tosyl-1H-indol-3-yl)methyl)-2,9-diazaspiro[5.5]undecane-9-carboxylate
DOI: 10.6084/m9.figshare.5104873.v1
Cc1ccc(S(=O)(=O)n2cc(CN3CCCC4(CCNCC4)C3=O)c3ccccc32)cc1
Reaction #69851
title compound
Ausbeute 144.1%DOI: 10.6084/m9.figshare.5104873.v1
O=C1CC2(CCCC2)CC(=O)N1CCN1CCN(c2ccccc2F)CC1
Reaction #77311
title compound
Ausbeute 40.3%DOI: 10.6084/m9.figshare.5104873.v1
CS(=O)(=O)c1ccccc1-c1ccc(N2CCCC(Nc3ccc(F)c(C(=N)NO)c3)C2=O)c(F)c1
Reaction #78318
title compound
Ausbeute 72.0%DOI: 10.6084/m9.figshare.5104873.v1
CC1(N2Cc3cc(Br)ccc3C2=O)CCC(=O)NC1=O
Reaction #91694
3-(5-bromo-1-oxo-1,3-dihydro-isoindol-2-yl)-3-methyl-piperidine-2,6-dione
Ausbeute 61.0%DOI: 10.6084/m9.figshare.5104873.v1
O=C(Cc1ccc(SC(F)(F)F)cc1)NCc1ccc2c(c1)CN(C1CCC(=O)NC1=O)C2=O
Reaction #91706
N-[2-(2,6-dioxo-piperidin-3-yl)-1-oxo-2,3-dihydro-1H-isoindol-5-ylmethyl]-2-(4-trifluoromethylsulfanyl-phenyl)-acetamide
Ausbeute 46.0%DOI: 10.6084/m9.figshare.5104873.v1
O=C1CCC(N2Cc3cc(CNC(=O)Nc4ccc(SC(F)(F)F)cc4)ccc3C2=O)C(=O)N1
Reaction #91778
1-[2-(2,6-dioxo-piperidin-3-yl)-1-oxo-2,3-dihydro-1H-isoindol-5-ylmethyl]-3-(4-trifluoromethylsulfanyl-phenyl)-urea
Ausbeute 51.0%DOI: 10.6084/m9.figshare.5104873.v1
O=C1CCC(N2Cc3cc(CNC(=S)Nc4ccc(SC(F)(F)F)cc4)ccc3C2=O)C(=O)N1
Reaction #91779
1-[2-(2,6-dioxo-piperidin-3-yl)-1-oxo-2,3-dihydro-1H-isoindol-5-ylmethyl]-3-(4-trifluoromethylsulfanyl-phenyl)-thiourea
Ausbeute 48.0%DOI: 10.6084/m9.figshare.5104873.v1
CC1C2CN(C)CC12c1ccccc1.Cl
Reaction #94566
title product
DOI: 10.6084/m9.figshare.5104873.v1
CCCc1cccc(-c2cc(NC(=O)C34CC3C(=O)N(Cc3ccc(OC)cc3OC)C4)nn2-c2ccccc2)c1
Reaction #170761
titled compound
Ausbeute 90.7%DOI: 10.6084/m9.figshare.5104873.v1
CCCc1cccc(-c2cc(NC(=O)C34CNC(=O)C3C4)nn2-c2ccccc2)c1
Reaction #170762
titled compound
Ausbeute 6.5%DOI: 10.6084/m9.figshare.5104873.v1
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