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774565

Cl.N=C(NCCCCc1ccc(O)cc1)NC(=O)c1nc(Cl)c(N)nc1N
Reaction #53369
4-(4-Hydroxyphenyl)butylamidino-3,5-diamino-6-chloropyrazinecarboxamide hydrochloride
DOI: 10.6084/m9.figshare.5104873.v1
Cl.N=C(NCCCCc1ccc(O)cc1)NC(=O)c1nc(Cl)c(N)nc1N
Reaction #53374
5
Ausbeute 84.4%DOI: 10.6084/m9.figshare.5104873.v1
Cl.N=C(NCCCc1ccc(O)cc1)NC(=O)c1nc(Cl)c(N)nc1N
Reaction #53377
compound 15
Ausbeute 60.0%DOI: 10.6084/m9.figshare.5104873.v1
Cl.N=C(NCCCCCc1ccc(O)cc1)NC(=O)c1nc(Cl)c(N)nc1N
Reaction #53380
22
Ausbeute 131.5%DOI: 10.6084/m9.figshare.5104873.v1
Cl.N=C(NCCCCc1ccc(O)c(O)c1)NC(=O)c1nc(Cl)c(N)nc1N
Reaction #53384
compound 28
Ausbeute 51.0%DOI: 10.6084/m9.figshare.5104873.v1
Cl.N=C(NCCCCc1ccc(O)cc1O)NC(=O)c1nc(Cl)c(N)nc1N
Reaction #53391
81
Ausbeute 58.3%DOI: 10.6084/m9.figshare.5104873.v1
Cl.N=C(NCCCCc1ccc(CC(=O)O)cc1)NC(=O)c1nc(Cl)c(N)nc1N
Reaction #53395
9
Ausbeute 46.5%DOI: 10.6084/m9.figshare.5104873.v1
CC1(C)OCC(COc2ccc(CCCCNC(=N)NC(=O)c3nc(Cl)c(N)nc3N)cc2)O1
Reaction #53401
Compound 37
Ausbeute 185.6%DOI: 10.6084/m9.figshare.5104873.v1
Cl.N=C(NCCCCc1ccc(O)cc1)NC(=O)c1nc(Cl)c(N)nc1N
Reaction #53407
5
Ausbeute 84.4%DOI: 10.6084/m9.figshare.5104873.v1
Cl.N=C(NCCCCc1ccc(CO)cc1)NC(=O)c1nc(Cl)c(N)nc1N
Reaction #53411
68
Ausbeute 194.0%DOI: 10.6084/m9.figshare.5104873.v1
CCCCNC(=N)NC(=O)c1nc(Cl)c(N)nc1N.Cl
Reaction #53420
compound 116
Ausbeute 194.0%DOI: 10.6084/m9.figshare.5104873.v1
Cl.N=C(NCCCCc1ccc(OCCN)cc1)NC(=O)c1nc(Cl)c(N)nc1N
Reaction #53421
4-[4-(2-aminoethyloxy)pheny)butylamidino-3,5-diamino-6-chloropyrazinecarboxamide hydrochloride
DOI: 10.6084/m9.figshare.5104873.v1
Cl.N=C(NCCCCc1ccc(CC(=O)O)cc1)NC(=O)c1nc(Cl)c(N)nc1N
Reaction #168478
9
Ausbeute 46.5%DOI: 10.6084/m9.figshare.5104873.v1
CC1(C)OCC(COc2ccc(CCCCNC(=N)NC(=O)c3nc(Cl)c(N)nc3N)cc2)O1
Reaction #168484
Compound 37
Ausbeute 185.6%DOI: 10.6084/m9.figshare.5104873.v1
Cl.N=C(NCCCCc1ccc(O)cc1)NC(=O)c1nc(Cl)c(N)nc1N
Reaction #168488
5
Ausbeute 84.4%DOI: 10.6084/m9.figshare.5104873.v1
Cl.N=C(NCCCCc1ccc(CO)cc1)NC(=O)c1nc(Cl)c(N)nc1N
Reaction #168492
68
Ausbeute 194.0%DOI: 10.6084/m9.figshare.5104873.v1
Cl.N=C(NCCCCc1ccc(OCCN)cc1)NC(=O)c1nc(Cl)c(N)nc1N
Reaction #168501
4-[4-(2-aminoethyloxy)phenyl)butylamidino-3,5-diamino-6-chloropyrazinecarboxamide hydrochloride
DOI: 10.6084/m9.figshare.5104873.v1
N=C(NCCCCc1ccc(OCCN)cc1)NC(=O)c1nc(Cl)c(N)nc1N
Reaction #168505
product
Ausbeute 125.9%DOI: 10.6084/m9.figshare.5104873.v1
Cl.Cl.N=C(N)NCCOc1ccc(CCCCNC(=N)NC(=O)c2nc(Cl)c(N)nc2N)cc1
Reaction #168506
pure product
Ausbeute 96.0%DOI: 10.6084/m9.figshare.5104873.v1
Cl.Cl.N=C(NCCCCc1ccc(OCCN(C[C@@H](O)[C@H](O)[C@H](O)CO)C[C@@H](O)[C@H](O)[C@H](O)CO)cc1)NC(=O)c1nc(Cl)c(N)nc1N
Reaction #168514
compound 23
Ausbeute 20.6%DOI: 10.6084/m9.figshare.5104873.v1
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