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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1954843Erstellt: 27. Oktober 2026

2-Amino-2-methyl-1,3-propanediol → N,N'-bis-(1,3-dihydroxy-2-methylprop-2-yl)pyrazine-2,3-dicarboxamide

https://huagongshe.com/reaction/1954843

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt2-Amino-2-methyl-1,3-propanediolHCID 1531—
Edukt4-MethylmorpholineHCID 7972—
Edukt2,3-Pyrazinedicarboxylic acidHCID 66628—
Edukt1-HydroxybenzotriazoleHCID 75771—
EduktPyBOPHCID 2724699—
LösungsmittelDimethylformamideHCID 6228—
LösungsmittelAcetonitrileHCID 6342—
LösungsmittelTrifluoroacetic acidHCID 6422—
ProduktN,N'-bis-(1,3-dihydroxy-2-methylprop-2-yl)pyrazine-2,3-dicarboxamideHCID 23293754—

Reaktionsschritte

Pyrazine-2,3-dicarboxylic acid (34 mg, 0.2 mmol), PyBOP (229 mg, 0.44 mmol), HOBt (60 mg, 0.44 mmol) and NMM (0.7 mL, 0.64 mmol) were dissolved in DMF (2 mL) and allowed to react for 10 min. 2-Amino-2-methyl-1,3-propanediol (46 mg, 0.44 mmol) was then added and stirring was continued overnight. The entire reaction mixture was then fractionated on a RP-HPLC column (Vydac 218TP1022, 22×250 mm, 10 mL/min, 0 to 15% MeCN in 0.1% aq CF3COOH over 40 min). Appropriate fractions were pooled, rechromatographed and lyophilised to yield the pure title compound. Alternatively, the title compound was synthesised as follows: dimethylpyrazine-2,3-dicarboxylate (1.5 g, 7.7 mmol) and 2-amino-2-methyl-1,3-propanediol (1.6 g, 15.4 mmol) in absolute ethanol (5 mL) were heated under reflux during 4 hours. The reaction mixture was then cooled and the solvent was removed under reduced pressure. The residue was chromatographed on a flash silica gel column using CHCl3 /MeOH (4:1) as the eluant. Solvents were removed in vacua and the pure title compound (2.2 g, 85%) was obtained after recrystallisation from isopropanol/hexane.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS06124298
Quelldatensatzuspto-grants-2000_09
ORD IDord-da604404412144d49af83901be92b4cb
Quellennotizuspto-grants-2000_09