Stannous Chloride → 4-(4-Dimethylaminomethyl-[1,2,3]triazol-1-yl)-phenylamine
Reaktionsgleichung
[N:1]1C=CC=CC=1C1N=NN(C2C=CC(NC3C4N(C=CN=4)C(C4C=CC(C(N)=O)=CC=4)=CN=3)=CC=2)C=1.[CH3:37][N:38]([CH3:54])[CH2:39][C:40]1[N:41]=[N:42][N:43]([C:45]2[CH:50]=[CH:49][C:48]([N+:51]([O-])=O)=[CH:47][CH:46]=2)[CH:44]=1.[Sn](Cl)Cl>C1COCC1.CCO>[NH3:1].[CH3:54][N:38]([CH2:39][C:40]1[N:41]=[N:42][N:43]([C:45]2[CH:46]=[CH:47][C:48]([NH2:51])=[CH:49][CH:50]=2)[CH:44]=1)[CH3:37]Komponenten
6
Edukt 3
Produkt 2
Reagenzien, Katalysatoren, Lösungsmittel 1
Versuchsvorschrift
In the same way as described for Compound 154, step 2 using dimethyl-[1-(4-nitro-phenyl)-1H-[1,2,3]triazol-4-ylmethyl]-amine (0.178 g, 0.722 mmol), tin(II) chloride dehydrate (0.578 g, 2.54 mmol) in (1:1) THF/EtOH (4 mL). The residue is purified on Isolute FlashSilicaII cartridge eluting with 95:5 DCM:NH3 (7M in MeOH), to afford the desired compound as a yellow solid (93.2 mg, 59%).
Aufarbeitung
- customThe residue is purified on Isolute FlashSilicaII cartridge
- washeluting with 95:5 DCM
Quellen und Nachweise
- ORD-Eintrag
- ord-0770370d7f614523ad29a6beba17d3d4
- Quelldatensatz
- uspto-grants-2012_05
- Patentnummer
- US08173656B2
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