Reaktionsgleichung
[CH3:1][NH:2][CH3:3].[CH2:4]=O.[S:6]1[C:13]2[CH:12]=[C:11]([C:14]([O:16][CH3:17])=[O:15])[NH:10][C:9]=2[CH:8]=[CH:7]1.[OH-].[Na+]>C(O)(=O)C>[CH3:1][N:2]([CH2:4][C:12]1[C:13]2[S:6][CH:7]=[CH:8][C:9]=2[NH:10][C:11]=1[C:14]([O:16][CH3:17])=[O:15])[CH3:3]Komponenten
Edukt 4
Produkt 1
Reagenzien, Katalysatoren, Lösungsmittel 1
Versuchsvorschrift
Under N2, to 9 mL of glacial acetic acid were added N,N-dimethylamine (40% aqueous solution) (437 mg, 9.94 mmol), formaldehyde (37% aqueous solution) (283 mg, 9.90 mmol), and methyl 4H-thieno[3,2-b]pyrrole-5-carboxylate (1.8 g, 9.94 mmol). The temperature was kept between 0-5° C. while the components were added. The reaction mixture was heated at reflux for 1 h, and then allowed to stand at rt for 12 h. The mixture was poured onto 30 g of ice, and was brought to pH 10 by careful addition of 10% sodium hydroxide. The temperature was not allowed to exceed 10° C. while the base was added. The gummy substance that precipitated solidified when stored in the refrigerator overnight. The solid was collected and dried in a vacuum. It was recrystallized from petroleum ether (30-60° C.) to yield methyl 6-[(dimethylamino)methyl]-4H-thieno[3,2-b]pyrrole-5-carboxylate (1.65 g, 70%). 1H NMR (400 MHz, CDCl3) δ ppm 2.36 (s, 6H) 3.86 (s, 3H) 3.89 (s, 2H) 6.85 (d, J=5.32 Hz, 1H) 7.28 (d, J=5.32 Hz, 1H) 9.84 (s, 1H).
Aufarbeitung
- customwas kept between 0-5° C. while the components
- additionwere added
- temperatureThe reaction mixture was heated
- temperatureat reflux for 1 h
- customto exceed 10° C. while the base
- additionwas added
- customThe gummy substance that precipitated
- customstored in the refrigerator overnight
- customThe solid was collected
- customdried in a vacuum
- customIt was recrystallized from petroleum ether (30-60° C.)
Quellen und Nachweise
- ORD-Eintrag
- ord-3a3fa57e64cd4d78b6cd4424a86186d1
- Quelldatensatz
- uspto-grants-2011_02
- Patentnummer
- US07884124B2
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