Triethylamine → HCID 18940670, Verbindung
Reaktionsgleichung
[N:1]1[CH:6]=[CH:5][CH:4]=[CH:3][C:2]=1[C:7]1[S:11][C:10]([C:12]([OH:14])=O)=[CH:9][CH:8]=1.C(N(CC)CC)C.[CH3:22][O:23][C:24]1[CH:29]=[CH:28][C:27]([NH2:30])=[CH:26][C:25]=1[N:31]1[CH2:36][CH2:35][N:34]([CH3:37])[CH2:33][CH2:32]1>S(Cl)(Cl)=O>[CH3:22][O:23][C:24]1[CH:29]=[CH:28][C:27]([NH:30][C:12]([C:10]2[S:11][C:7]([C:2]3[CH:3]=[CH:4][CH:5]=[CH:6][N:1]=3)=[CH:8][CH:9]=2)=[O:14])=[CH:26][C:25]=1[N:31]1[CH2:32][CH2:33][N:34]([CH3:37])[CH2:35][CH2:36]1Komponenten
Edukt 3
Produkt 1
Reagenzien, Katalysatoren, Lösungsmittel 1
Versuchsvorschrift
5-(pyrid-2-yl)thiophene-2-carboxylic acid (0.279 g; 1.36 mmol) was heated at reflux in thionyl chloride (8 ml) for 1 hour, cooled, evaporated in vacuo and the residue azeotroped with toluene. The orange residue was redissolved in CH2Cl2 (10 ml) and treated with dry triethylamine (0.19 ml; 1.36 mmol) and 4-methoxy-3-(4-methyl-1-piperazinyl)benzenamine (0.3 g;1.36 mmol). The solution was stirred under Ar (18 hours), evaporated in vacuo and partitioned satd. K2CO3 (aq)/EtOAc. The organic phases were combined, dried over Na2SO4, filtered and the filtrate evaporated in vacuo to a brown gum. The gum was purified by flash silica-gel chromatography and eluted with 2%MeOH/CHCl3 to yield the title compound as a orange gum (0.37 g;67%), which was converted to the oxalate salt, mp=131° C.(dec).
Aufarbeitung
- temperaturecooled
- customevaporated in vacuo
- customthe residue azeotroped with toluene
- dissolutionThe orange residue was redissolved in CH2Cl2 (10 ml)
- customevaporated in vacuo
- custompartitioned
- dry with materialdried over Na2SO4
- filtrationfiltered
- customthe filtrate evaporated in vacuo to a brown gum
- customThe gum was purified by flash silica-gel chromatography
- washeluted with 2%MeOH/CHCl3
Quellen und Nachweise
- ORD-Eintrag
- ord-d0afb57847b44626ad5bc306747eb2e6
- Quelldatensatz
- uspto-grants-1998_11
- Patentnummer
- US05834471
Notizen zur Reaktion
Wird geladen…