Hydrochloric Acid → 5-bromo-N-(2-aminoethyl)-2-thiophenecarboxamide hydrochloride
Reaktionsgleichung
[NH:1]([CH2:5][CH2:6][NH:7][C:8]([C:10]1[S:11][C:12]([Br:15])=[CH:13][CH:14]=1)=[O:9])C(C)=O.[ClH:16]>>[ClH:16].[Br:15][C:12]1[S:11][C:10]([C:8]([NH:7][CH2:6][CH2:5][NH2:1])=[O:9])=[CH:14][CH:13]=1Komponenten
3
Versuchsvorschrift
N-(2-Acetaminoethyl)-5-bromo-2-thiophenecarboxamide was reacted with hydrochloric acid in an analogous manner to that described in Example 1, paragraph 3. The residue was dissolved in alcohol (pH 1), filtered and concentrated to about 300 ml under reduced pressure. After cooling to 5° the product was filtered off under suction and dried, whereby 5-bromo-N-(2-aminoethyl)-2-thiophenecarboxamide hydrochloride was obtained as white crystals, m.p. 221°-222°, after recrystallization from ethanol.
Aufarbeitung
- filtrationfiltered
- concentrationconcentrated to about 300 ml under reduced pressure
- temperatureAfter cooling to 5° the product
- filtrationwas filtered off under suction
- customdried
Quellen und Nachweise
- ORD-Eintrag
- ord-54ae05bc05c541b0a898ca7dc86540e6
- Quelldatensatz
- uspto-grants-1988_08
- Patentnummer
- US04764522
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