Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1954843Generated: October 25, 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

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-Amino-2-methyl-1,3-propanediolHCID 1531—
Reactant4-MethylmorpholineHCID 7972—
Reactant2,3-Pyrazinedicarboxylic acidHCID 66628—
Reactant1-HydroxybenzotriazoleHCID 75771—
ReactantPyBOPHCID 2724699—
SolventDimethylformamideHCID 6228—
SolventAcetonitrileHCID 6342—
SolventTrifluoroacetic acidHCID 6422—
ProductN,N'-bis-(1,3-dihydroxy-2-methylprop-2-yl)pyrazine-2,3-dicarboxamideHCID 23293754—

Reaction Steps

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.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06124298
Source datasetuspto-grants-2000_09
ORD IDord-da604404412144d49af83901be92b4cb
Source noteuspto-grants-2000_09