2-Morpholinoethylamine → HCID 178523408, Verbindung
Reaktionsgleichung
CO[C:3]([C:5]1[N:10]=[CH:9][C:8]2[N:11]=[CH:12][NH:13][C:7]=2[CH:6]=1)=[O:4].[N:14]1([CH2:20][CH2:21][NH2:22])[CH2:19][CH2:18][O:17][CH2:16][CH2:15]1>CO>[N:14]1([CH2:20][CH2:21][NH:22][C:3]([C:5]2[N:10]=[CH:9][C:8]3[N:11]=[CH:12][NH:13][C:7]=3[CH:6]=2)=[O:4])[CH2:19][CH2:18][O:17][CH2:16][CH2:15]1Komponenten
4
Edukt 2
Produkt 1
Reagenzien, Katalysatoren, Lösungsmittel 1
Versuchsvorschrift
2.0 g of methyl-1H-imidazo[4,5-c]pyridine-6-carboxylate (example D2), 22.1 g of 2-morpholin-4-ylethanamine and 70 ml methanol were placed in an autoclave for 2 h at 140° C. The methanol and 2-morpholin-4-ylethanamine were distilled off the reaction mixture under reduced pressure and the residue was purified by flash chromatography. After crystallization from ethyl acetate/n-hexane the title compound was obtained.
Aufarbeitung
- distillationThe methanol and 2-morpholin-4-ylethanamine were distilled off the reaction mixture under reduced pressure
- customthe residue was purified by flash chromatography
- customAfter crystallization from ethyl acetate/n-hexane the title compound
- customwas obtained
Quellen und Nachweise
- ORD-Eintrag
- ord-35acffd2cafc42578e25feb441b6838f
- Quelldatensatz
- uspto-grants-2012_09
- Patentnummer
- US08273890B2
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