Methanol → 3-(2-Amino-4-thiazolyl)alanine
Reaktionsgleichung
N[C@H](C(O)=O)CCC(O)=O.[NH2:11][C:12]1[S:13][CH:14]=[C:15]([CH2:17][C@@H:18]([C:20]([OH:22])=[O:21])[NH2:19])[N:16]=1.CO>C(N(CC)CC)C>[NH2:11][C:12]1[S:13][CH:14]=[C:15]([CH2:17][C@@H:18]([C:20]([OH:22])=[O:21])[NH2:19])[N:16]=1Komponenten
4
Edukt 2
Produkt 1
Reagenzien, Katalysatoren, Lösungsmittel 1
Reaktionsbedingungen
- Temperatur
- 5 °C
Versuchsvorschrift
3-(2-Amino-4-thiazolyl)-L-alanine L-glutamic acid salt, 37.6 kg (112 mol) and 420 L of methanol are charged into a reactor and stirred as 34.4 kg of triethylamine is added. The slurry is heated to reflux for 1 hour and then cooled to 5° C. The product is filtered, washed with 25 L of methanol to give 26.3 kg of 3-(2-amino-4-thiazolyl)-L-alanine as a white solid containing methanol. A dried sample is >99% pure and >99% enantiomeric excess by chiral high pressure liquid chromatography (HPLC); IR (mineral oil): 3170 (s, br), 1618 (s), 1525 (s), 1108 (m) cm-1.
Aufarbeitung
- additionis added
- temperatureThe slurry is heated
- temperatureto reflux for 1 hour
- filtrationThe product is filtered
- washwashed with 25 L of methanol
Quellen und Nachweise
- ORD-Eintrag
- ord-0391cce40f1c4a00a23c0fe4d43a7e08
- Quelldatensatz
- uspto-grants-1992_02
- Patentnummer
- US05089616
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