Hydrochloric Acid → HCID 19093039, Verbindung
Reaktionsgleichung
[ClH:1].C([N:5]1[CH2:10][CH2:9][C:8]2[S:11][C:12]([C:15]([O:17][CH3:18])=[O:16])=[C:13]([NH2:14])[C:7]=2[CH2:6]1)(=O)C>CO>[ClH:1].[NH2:14][C:13]1[C:7]2[CH2:6][NH:5][CH2:10][CH2:9][C:8]=2[S:11][C:12]=1[C:15]([O:17][CH3:18])=[O:16]Komponenten
4
Edukt 2
Produkt 1
Reagenzien, Katalysatoren, Lösungsmittel 1
Versuchsvorschrift
20 ml of methanol and then 5.1 ml of concentrated hydrochloric acid were added to 2.54 g of methyl 5-acetyl-3-amino-4,5,6,7tetrahydrothieno[3,2-c]pyridine-2-carboxylate (Compound No. 16) obtained in Example 1. The resultant mixture was heated under reflux for 4 hours. After cooling, the crystals thus formed were taken by filtration to obtain 1.70 g (68%) of methyl 3-amino-4,5,6,7-tetrahydrothieno[3,2-c]pyridine-2-carboxylate hydrochloride.
Aufarbeitung
- custom16) obtained in Example 1
- temperatureunder reflux for 4 hours
- temperatureAfter cooling
- customthe crystals thus formed
- filtrationwere taken by filtration
Quellen und Nachweise
- ORD-Eintrag
- ord-a0bc80d4251f45c3b78165ddbb33391a
- Quelldatensatz
- uspto-grants-1994_03
- Patentnummer
- US05296603
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