Dimethylamine → N-[4-[(Dimethylamino)methyl]-2-thiazolyl]acetamide
Reaktionsgleichung
Cl[CH2:2][C:3]1[N:4]=[C:5]([NH:8][C:9](=[O:11])[CH3:10])[S:6][CH:7]=1.C([O-])([O-])=O.[Na+].[Na+].[CH3:18][NH:19][CH3:20]>C1COCC1>[CH3:18][N:19]([CH2:2][C:3]1[N:4]=[C:5]([NH:8][C:9](=[O:11])[CH3:10])[S:6][CH:7]=1)[CH3:20]Komponenten
5
Edukt 3
Produkt 1
Reagenzien, Katalysatoren, Lösungsmittel 1
Reaktionsbedingungen
- Temperatur
- 50 °C
Versuchsvorschrift
Dissolved N-(4-chloromethyl-thiazol-2-yl)-acetamide (250 mg, 1.31 mmol) in 5 mL of THF. To this was added Na2CO3 (250 mg). Bubbled dimethyl amine in for 15 min. Sealed the flask and heated at 50° C. for 2 h. LC-MS analysis indicated the desired adduct. Filtered the mixture through diatomaceous earth and washed plug with 2×10 mL of THF. Concentrated to dryness to give 274 mg of N-(4-dimethylaminomethyl-thiazol-2-yl)-acetamide.
Aufarbeitung
- customin for 15 min
- customSealed the flask
- filtrationFiltered the mixture through diatomaceous earth
- washwashed plug with 2×10 mL of THF
- concentrationConcentrated to dryness
Quellen und Nachweise
- ORD-Eintrag
- ord-f7d49d438ca14202acabd2406b850de1
- Quelldatensatz
- uspto-grants-2012_01
- Patentnummer
- US08093266B2
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