Hydrochloric Acid → (2S)-piperazine-2-carboxylic acid dihydrochloride
Reaktionsgleichung
[NH:1]1[CH2:6][CH2:5][NH:4][CH2:3][C@H:2]1[C:7]([O:9]C(C)(C)C)=[O:8].[ClH:14]>O>[ClH:14].[ClH:14].[NH:1]1[CH2:6][CH2:5][NH:4][CH2:3][C@H:2]1[C:7]([OH:9])=[O:8]Komponenten
4
Edukt 2
Produkt 1
Reagenzien, Katalysatoren, Lösungsmittel 1
Reaktionsbedingungen
- Temperatur
- 0 °C
Versuchsvorschrift
The crude tert-butyl (S)-piperazine-2-carboxylate from Example 7 was stirred in 2.9 g of water and 2.1 g (18.4 mmol) of 32 percent hydrochloric acid for 20 minutes at 100° C. The mixture was cooled to 0° C. and stirred for a further 1 hour. The hydrochloride which had precipitated out was filtered off and washed with 10 ml of dichloromethane. The yield of the title compound was 0.24 g (41 percent, based on tert-butyl pyrazinecarboxylate). The ee value was 77.6 percent.
Aufarbeitung
- customThe hydrochloride which had precipitated out
- filtrationwas filtered off
- washwashed with 10 ml of dichloromethane
Quellen und Nachweise
- ORD-Eintrag
- ord-0ee039259ffc44829d7a2b491a05c2bb
- Quelldatensatz
- uspto-grants-1999_08
- Patentnummer
- US05945534
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