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466

O=C(O)c1cc(F)c(F)c(Cl)c1NC1CC1
Reaction #10398
title compound
Ausbeute 63.7%DOI: 10.6084/m9.figshare.5104873.v1
Cc1c(CC(N)=O)ccc(C#N)c1Cl
Reaction #43461
nitrile
Ausbeute 67.0%DOI: 10.6084/m9.figshare.5104873.v1
—
Reaction #44397
hydrochloride salt
Ausbeute 75.0%DOI: 10.6084/m9.figshare.5104873.v1
N[C@@H]1CCC(c2cccc(Cl)c2Cl)CNC1=O
Reaction #48398
title compound
Ausbeute 176.3%DOI: 10.6084/m9.figshare.5104873.v1
Clc1ccc(Nc2cc3c4c(c2)[C@@H]2CNCC[C@@H]2N4CCSC3)c(Cl)c1
Reaction #51542
title compound
Ausbeute 61.9%DOI: 10.6084/m9.figshare.5104873.v1
Clc1cccc(Nc2cc3c4c(c2)[C@@H]2CNCC[C@@H]2N4CCSC3)c1Cl
Reaction #51543
title compound
DOI: 10.6084/m9.figshare.5104873.v1
FC(F)(F)c1ccc(Cl)c(Nc2cc3c4c(c2)[C@@H]2CNCC[C@@H]2N4CCSC3)c1
Reaction #51544
title compound
DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)c1c(Cl)cc(N)c(Br)c1Cl
Reaction #52999
2,6-dichloro-3-bromo-4-aminobenzoic acid methyl ester
Ausbeute 139.4%DOI: 10.6084/m9.figshare.5104873.v1
Clc1ccc(Nc2cc3c4c(c2)[C@@H]2CNCC[C@@H]2N4CCSC3)c(Cl)c1
Reaction #75824
title compound
Ausbeute 61.9%DOI: 10.6084/m9.figshare.5104873.v1
Clc1cccc(Nc2cc3c4c(c2)[C@@H]2CNCC[C@@H]2N4CCSC3)c1Cl
Reaction #75825
title compound
DOI: 10.6084/m9.figshare.5104873.v1
FC(F)(F)c1ccc(Cl)c(Nc2cc3c4c(c2)[C@@H]2CNCC[C@@H]2N4CCSC3)c1
Reaction #75826
title compound
DOI: 10.6084/m9.figshare.5104873.v1
O=[N+]([O-])c1cc(F)c(Cl)c(Br)c1Cl
Reaction #76178
3-bromo-2,4-dichloro-5-fluoronitrobenzene
Ausbeute 91.9%DOI: 10.6084/m9.figshare.5104873.v1
COc1c(Cl)c(F)cc([N+](=O)[O-])c1Cl
Reaction #76179
2,4-dichloro-5-fluoro-3-methoxynitrobenzene
Ausbeute 728.6%DOI: 10.6084/m9.figshare.5104873.v1
O=C(CCl)c1cc(F)c(Cl)c(F)c1Cl
Reaction #76186
3,5-difluoro-2,4,6-trichloroacteylbenzene
Ausbeute 81.9%DOI: 10.6084/m9.figshare.5104873.v1
CCOc1ccc(Br)c(Cl)c1
Reaction #79299
1-bromo-2-chloro-4-ethoxybenzene
Ausbeute 81.2%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)Oc1ccc(Br)c(Cl)c1
Reaction #79301
1-bromo-2-chloro-4-isopropoxybenzene
Ausbeute 81.0%DOI: 10.6084/m9.figshare.5104873.v1
O=[N+]([O-])c1cc(Cl)c(Br)cc1Cl
Reaction #82090
pure title compound
Ausbeute 95.0%DOI: 10.6084/m9.figshare.5104873.v1
O=C1CNc2cc(Br)c(Cl)cc2N1
Reaction #82092
pure title compound
Ausbeute 18.0%DOI: 10.6084/m9.figshare.5104873.v1
O=c1cnc2c([N+](=O)[O-])c(Br)c(Cl)cc2[nH]1
Reaction #82093
title compound
Ausbeute 70.0%DOI: 10.6084/m9.figshare.5104873.v1
Nc1c(Cl)c(Br)cc2[nH]c(=O)c(=O)[nH]c12
Reaction #82098
pure title compound
Ausbeute 62.0%DOI: 10.6084/m9.figshare.5104873.v1
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