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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1954843생성일: 2026년 10월 27일

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

반응식

참여 물질

역할이름HCID투입량
반응물2-Amino-2-methyl-1,3-propanediolHCID 1531—
반응물4-MethylmorpholineHCID 7972—
반응물2,3-Pyrazinedicarboxylic acidHCID 66628—
반응물1-HydroxybenzotriazoleHCID 75771—
반응물PyBOPHCID 2724699—
용매DimethylformamideHCID 6228—
용매AcetonitrileHCID 6342—
용매Trifluoroacetic acidHCID 6422—
생성물N,N'-bis-(1,3-dihydroxy-2-methylprop-2-yl)pyrazine-2,3-dicarboxamideHCID 23293754—

반응 단계

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.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06124298
출처 데이터셋uspto-grants-2000_09
ORD IDord-da604404412144d49af83901be92b4cb
출처 메모uspto-grants-2000_09