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765656

Cc1nc2n(C)c3ccccc3n2c1C(=O)C(Cl)(Cl)Cl
Reaction #82977
2,9-Dimethyl-3-trichloroacetylimidazo[1,2-a]benzimidazole
DOI: 10.6084/m9.figshare.5104873.v1
O=C1c2cnc3cccc(n23)CN1c1ccc(CCNS(=O)(=O)C(F)(F)F)cc1
Reaction #202742
DOI: 10.1039/C8SC04228D
CCOC(=O)c1cccc2ncc(C(=O)C(Cl)(Cl)Cl)n12
Reaction #225163
DOI: 10.1039/C8SC04228D
CC(C)(C)OC(=O)N(CCCNS(=O)(=O)C(F)(F)F)Cc1cccc2ncc(C(=O)C(Cl)(Cl)Cl)n12
Reaction #225338
DOI: 10.1039/C8SC04228D
CC(C)(C)OC(=O)N(CCCCCNS(=O)(=O)C(F)(F)F)Cc1cccc2ncc(C(=O)C(Cl)(Cl)Cl)n12
Reaction #235878
DOI: 10.1039/C8SC04228D
CCCSc1ncc(CCC(C(=O)OCC)C(=O)OCC)n1Cc1ccccc1Cl
Reaction #243350
DOI: 10.1039/C8SC04228D
O=C1c2cnc3cccc(n23)CN1CCCCCNS(=O)(=O)C(F)(F)F
Reaction #264515
DOI: 10.1039/C8SC04228D
CCc1nc2cccc3n2c1C(=O)N(CCCCCNS(=O)(=O)C(F)(F)F)C3
Reaction #288491
DOI: 10.1039/C8SC04228D
Cc1ccc(-c2nc3ccc(C)cn3c2CC(=O)Cl)cc1.Cl
Reaction #317428
title compound
Ausbeute 118.2%DOI: 10.6084/m9.figshare.5104873.v1
CCCSc1ncc(CCC(C(=O)OCC)C(=O)OCC)n1Cc1ccccc1Cl
Reaction #347932
title compound
Ausbeute 71.0%DOI: 10.6084/m9.figshare.5104873.v1
O=C(c1cnc2cccc(Cl)n12)C(Cl)(Cl)Cl
Reaction #402007
DOI: 10.1039/C8SC04228D
CC(=O)OC[C@H]1O[C@@H](n2cnc(C(=O)CCl)c2N)[C@H](Cl)[C@@H]1OC(C)=O
Reaction #442694
titled compound ( 39 )
DOI: 10.6084/m9.figshare.5104873.v1
CC(=O)OC[C@H]1O[C@@H](n2cnc(C(=O)CN=[N+]=[N-])c2N)[C@H](Cl)[C@@H]1OC(C)=O
Reaction #442695
titled compound ( 40 )
Ausbeute 92.0%DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc2cccc(CCNC(=O)Cc3c[nH]cn3)c2c1
Reaction #570581
N-[2-(7-Methoxynaphth-1-Yl)Ethyl]-4-Imidazolylacetamide
DOI: 10.6084/m9.figshare.5104873.v1
O=C1c2cnc3cccc(n23)CN1CCCCNS(=O)(=O)C(F)(F)F
Reaction #706611
desired compound
Ausbeute 65.1%DOI: 10.6084/m9.figshare.5104873.v1
O=C1c2cnc3cccc(n23)CN1CCCNS(=O)(=O)C(F)(F)F
Reaction #706613
desired compound
Ausbeute 54.8%DOI: 10.6084/m9.figshare.5104873.v1
O=C1c2cnc3cccc(n23)CN1CCCCCNS(=O)(=O)C(F)(F)F
Reaction #706614
object product
Ausbeute 63.1%DOI: 10.6084/m9.figshare.5104873.v1
Cc1nc2cccc(CN(CCCCNS(=O)(=O)C(F)(F)F)C(=O)OC(C)(C)C)n2c1C(=O)C(Cl)(Cl)Cl
Reaction #706615
desired compound
Ausbeute 65.2%DOI: 10.6084/m9.figshare.5104873.v1
CCc1nc2cccc(CN(CCCCCNS(=O)(=O)C(F)(F)F)C(=O)OC(C)(C)C)n2c1C(=O)C(Cl)(Cl)Cl
Reaction #706616
desired compound
Ausbeute 55.2%DOI: 10.6084/m9.figshare.5104873.v1
CCc1nc2cccc3n2c1C(=O)N(CCCCCNS(=O)(=O)C(F)(F)F)C3
Reaction #706617
desired compound
Ausbeute 53.2%DOI: 10.6084/m9.figshare.5104873.v1
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