DL-alanine → 2,3-Dicyano-5-(1-carboxyethyl)amino-6-phenylpyrazine

HRID 128397

Reaktionsgleichung

Reaktionsgleichung von HRID 128397
[C:1]([C:3]1[C:8]([C:9]#[N:10])=[N:7][C:6](Cl)=[C:5]([C:12]2[CH:17]=[CH:16][CH:15]=[CH:14][CH:13]=2)[N:4]=1)#[N:2].[CH3:18][CH:19]([NH2:23])[C:20]([OH:22])=[O:21].[OH-].[Na+].O>CC(C)=O>[C:1]([C:3]1[C:8]([C:9]#[N:10])=[N:7][C:6]([NH:23][CH:19]([C:20]([OH:22])=[O:21])[CH3:18])=[C:5]([C:12]2[CH:17]=[CH:16][CH:15]=[CH:14][CH:13]=2)[N:4]=1)#[N:2]

Komponenten

6

Edukt 4

HCID 602DL-alanineHCID 962WaterHCID 14798Sodium HydroxideHCID 129072055-Chloro-6-phenylpyrazine-2,3-dicarbonitrile

Produkt 1

HCID 133369692,3-Dicyano-5-(1-carboxyethyl)amino-6-phenylpyrazineAusbeute 42 %

Reagenzien, Katalysatoren, Lösungsmittel 1

HCID 180AcetoneLösungsmittel

Versuchsvorschrift

2,3-Dicyano-5-chloro-6-phenylpyrazine (4.82 g; 0.02 mole) was dissolved in 50 ml of acetone. The solution was cooled to 0° to 5° C., and with stirring, a solution prepared from 1.78 g (0.02 mole) of DL-α-alanine, 1.64 g (0.02 mole) of sodium hydroxide and 40 ml of water was added dropwise over the period of 30 minutes. The mixture was worked up in the same way as in Example 23, and recrystallized from benzene to afford 2.46 g (yield 42%) of 2,3-dicyano-5-(1-caroxyethyl)amino-6-phenylpyrazine.

Aufarbeitung

  1. temperatureThe solution was cooled to 0° to 5° C.
  2. additionwas added dropwise over the period of 30 minutes
  3. customrecrystallized from benzene

Quellen und Nachweise

ORD-Eintrag
ord-a2f9eef30b7e412db563be5317c91516
Quelldatensatz
uspto-grants-1981_03
Patentnummer
US04259489

Verknüpfte Notizen

Wird geladen…