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857567

COc1ccccc1NC(=O)c1ccc(C#N)cc1
Reaction #2512
title compound
Ausbeute 93.6%DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc(NC(=O)c2ccc(C#N)cc2)cc1
Reaction #2530
title compound
Ausbeute 91.7%DOI: 10.6084/m9.figshare.5104873.v1
CN(C)[C@@H]1CCCC[C@H]1NC(=O)c1ccc(C#N)cc1
Reaction #54532
amide
Ausbeute 63.0%DOI: 10.6084/m9.figshare.5104873.v1
CNC(=O)c1ccc(CNC(=O)[C@@H](CCCNC(N)=N[N+](=O)[O-])NC(=O)C(c2ccccc2)c2ccccc2)cc1
Reaction #80870
(R)-N5 -[Amino(nitroimino)methyl]-N2 -(diphenylacetyl)-N-[[4-[(methylamino)carbonyl]phenyl]methyl]-ornithinamide
Ausbeute 22.0%DOI: 10.6084/m9.figshare.5104873.v1
CC1(N2Cc3cc(C#N)ccc3C2=O)CCC(=O)NC1=O
Reaction #91695
2-(3-methyl-2,6-dioxo-piperidin-3-yl)-1-oxo-2,3-dihydro-1H-isoindole-5-carbonitrile
Ausbeute 99.0%DOI: 10.6084/m9.figshare.5104873.v1
CC1(N2Cc3cc(CN)ccc3C2=O)CCC(=O)NC1=O.Cl
Reaction #91696
3-(5-aminomethyl-1-oxo-1,3-dihydro-isoindol-2-yl)-3-methyl-piperidine-2,6-dione hydrochloride
Ausbeute 92.0%DOI: 10.6084/m9.figshare.5104873.v1
Cl.NCc1ccc2c(c1)C(=O)N(C1CCC(=O)NC1=O)C2=O
Reaction #91753
5-aminomethyl-2-(2,6-dioxo-piperidin-3-yl)-isoindole-1,3-dione hydrochloride
Ausbeute 85.0%DOI: 10.6084/m9.figshare.5104873.v1
N#Cc1ccc2c(c1)CN(C1CCC(=O)NC1=O)C2=O
Reaction #91760
2-(2,6-dioxo-piperidin-3-yl)-1-oxo-2,3-dihydro-1H-isoindole-5-carbonitrile
DOI: 10.6084/m9.figshare.5104873.v1
Cl.NCc1ccc2c(c1)CN(C1CCC(=O)NC1=O)C2=O
Reaction #91761
3-(5-aminomethyl-1-oxo-1,3-dihydro-isoindol-2-yl)-piperidine-2,6-dione hydrochloride
DOI: 10.6084/m9.figshare.5104873.v1
CCCOC(=O)[C@H](Cc1ccc(-c2c(C)n(C)c(=O)n(C)c2=O)cc1)NC(=O)c1c(F)cc(C#N)cc1F
Reaction #92024
(S)-2-(4-cyano-2,6-difluorobenzoylamino)-3-[4-(1,3,6-trimethyl-2,4-dioxo-1,2,3,4-tetrahydropyrimidin-5-yl)phenyl]propionic acid propyl ester
Ausbeute 99.0%DOI: 10.6084/m9.figshare.5104873.v1
CCCOC(=O)[C@H](Cc1ccc(-c2c(C)n(C)c(=O)n(C)c2=O)cc1)NC(=O)c1c(F)cc(CN)cc1F
Reaction #92025
(S)-2-(4-aminomethyl-2,6-difluorobenzoylamino)-3-[4-(1,3,6-trimethyl-2,4-dioxo-1,2,3,4-tetrahydropyrimidin-5-yl)phenyl]propionic acid propyl ester
Ausbeute 74.5%DOI: 10.6084/m9.figshare.5104873.v1
CCCOC(=O)[C@H](Cc1ccc(-c2c(C)n(C)c(=O)n(C)c2=O)cc1)NC(=O)c1c(F)cc(CNCc2cc(F)c(C(=O)N[C@@H](Cc3ccc(-c4c(C)n(C)c(=O)n(C)c4=O)cc3)C(=O)OCCC)c(F)c2)cc1F
Reaction #92029
title compound
Ausbeute 39.2%DOI: 10.6084/m9.figshare.5104873.v1
CCN(CC)C(=O)c1ccc(C#N)cc1F
Reaction #160148
4-cyano-N,N-diethyl-2-fluoro-benzamide
Ausbeute 75.0%DOI: 10.6084/m9.figshare.5104873.v1
CCN(CC)C(=O)c1ccc(C(=O)O)cc1F
Reaction #160149
4-(diethylcarbamoyl)-3-fluoro-benzoic acid
Ausbeute 66.0%DOI: 10.6084/m9.figshare.5104873.v1
N#Cc1ccc(C(=O)Nc2cccc(C(F)(F)F)c2)cc1-c1ccc2c(c1)[nH]c1ncncc12
Reaction #164899
TFA
DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc(N(Cc2cccc(C#N)n2)C2CCN(C(C)CCNC(=O)c3c(C)cc(C#N)cc3C)CC2)cc1
Reaction #175394
DOI: 10.1039/C8SC04228D
Cc1cc(C=O)cc2c1C(=O)N(Cc1ccc(OC(F)(F)F)cc1)C2
Reaction #180963
DOI: 10.1039/C8SC04228D
Cc1cc(Nc2nccc(NC(=O)c3c(Cl)cc(C#N)cc3Cl)c2[N+](=O)[O-])nc(C)n1
Reaction #181942
DOI: 10.1039/C8SC04228D
COc1ccccc1NC(=O)c1ccc(C#N)cc1
Reaction #186150
DOI: 10.1039/C8SC04228D
Cc1cc(C(F)(C(F)(F)F)C(F)(F)F)cc(C)c1NC(=O)c1ccc(C#N)c(F)c1F
Reaction #189427
DOI: 10.1039/C8SC04228D
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