Chloride → 7,8-bis(4-chlorophenyl)-2-ethyl-5-(pyridin-2-ylmethylamino)-[1,2,4]triazolo[4,3-c]pyrimidin-3(2H)-one
Reaktionsgleichung
Cl[C:2]1N2C(=O)NN=C2C(C2C=CC(Cl)=CC=2)=C(C2C=CC(Cl)=CC=2)N=1.[Cl-].ICC.[Cl:30][C:31]1[CH:36]=[CH:35][C:34]([C:37]2[N:42]=[C:41]([N:43]3[CH2:46][C:45]([NH:50][CH2:51][CH3:52])(C(N)=O)[CH2:44]3)[N:40]3[C:53](=[O:58])[N:54]([CH2:56][CH3:57])[N:55]=[C:39]3[C:38]=2[C:59]2[CH:64]=[CH:63][C:62]([Cl:65])=[CH:61][CH:60]=2)=[CH:33][CH:32]=1>>[Cl:30][C:31]1[CH:36]=[CH:35][C:34]([C:37]2[N:42]=[C:41]([NH:43][CH2:46][C:45]3[CH:44]=[CH:2][CH:52]=[CH:51][N:50]=3)[N:40]3[C:53](=[O:58])[N:54]([CH2:56][CH3:57])[N:55]=[C:39]3[C:38]=2[C:59]2[CH:60]=[CH:61][C:62]([Cl:65])=[CH:63][CH:64]=2)=[CH:33][CH:32]=1Komponenten
5
Edukt 4
Produkt 1
Versuchsvorschrift
The title compound was prepared in two steps from 5-chloro-7,8-bis(4-chlorophenyl)-[1,2,4]triazolo[4,3-c]pyrimidin-3(2H)-one by nucleophilic displacement of chloride with the requisite amine, followed by alkylation with iodoethane, in a manner analogous to that in which 1-(7,8-bis(4-chlorophenyl)-2-ethyl-3-oxo-2,3-dihydro-[1,2,4]triazolo[4,3-c]pyrimidin-5-yl)-3-(ethylamino)azetidine-3-carboxamide was prepared. HPLC/MS: retention time=3.623 min, [M+H]30 =491.
Aufarbeitung
- customwas prepared
Quellen und Nachweise
- ORD-Eintrag
- ord-5a9c18c8247a4b58a2d92636237376f0
- Quelldatensatz
- uspto-grants-2008_11
- Patentnummer
- US07452892B2
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