돌아가기
Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1823688생성일: 2026년 10월 27일

Isovaleryl chloride → 3-(3-Methyl-butyrylamino)-pyrazine-2-carboxylic acid

https://huagongshe.com/reaction/1823688

반응식

참여 물질

역할이름HCID투입량
반응물Isovaleryl chlorideHCID 66054—
반응물3-Amino-2-pyrazinecarboxylic acidHCID 72656—
반응물DiisopropylethylamineHCID 81531—
반응물3-(3-Methyl-butyrylamino)-pyrazine-2-carboxylic acid benzylamideHCID 69313458—
용매DimethylformamideHCID 6228—
생성물3-(3-Methyl-butyrylamino)-pyrazine-2-carboxylic acidHCID 22172602—

반응 단계

3-(3-Methyl-butyrylamino)-pyrazine-2-carboxylic acid benzylamide: To a solution of DMF (200 mL), 3-aminopyrazine-2-carboxylic acid (10.0 g, 71.9 mmol) and diisopropylethyl amine (25.0 mL, 144 mmol) was added isovaleryl chloride (12.4 mL, 86.3 mmol) dropwise at room temperature. The reaction mixture was stirred at room temperature for two hours after which the solvent was removed under reduced pressure and the residue dried under vacuum overnight, to afford 3-(3-methyl-butyrylamino)-pyrazine-2-carboxylic acid as a solid residue. The solid residue was dissolved in acetic anhydride (200 mL) and the mixture stirred at 100° C. overnight. The excess acetic anhydride was removed by distillation under reduced pressure, leaving a residue that was then cooled to room temperature and washed with hexane to give the corresponding oxazinone compound of Formula 103, 2-isobutyl-pyrazino[2,3-d][1,3]-oxazin-4-one, which was carried forward without additional purification. A solution of chloroform (200 mL), the oxazinone of Formula 103, and benzylamine (16.0 mL, 144 mmol) was stirred at 60° C. for two hours. After the complete consumption of the oxazinone, as monitored by reverse phase HPLC, the chloroform was removed under reduced pressure and the residue purified by silica gel chromatography using hexane-EtOAc (1:2) as eluent to obtain the title bis amide, 3-(3-methyl-butyrylamino)-pyrazine-2-carboxylic acid benzylamide (4.5 g 20.0%, three steps). MS (Cl) M/E: 313.1.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07038048B2
출처 데이터셋uspto-grants-2006_05
ORD IDord-4d0d54b4e7514cae8b346fa5c8b20e71
출처 메모uspto-grants-2006_05