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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 339488생성일: 2026년 10월 25일

Cyanogen Bromide → N2-[1-benzyl-2-(1-[(2-cyano-1,2-dimethylhydrazino)carbonyl]-3-methylbutylamino)-2-oxoethyl]-2-pyrazinecarboxamide

https://huagongshe.com/reaction/339488

반응식

참여 물질

역할이름HCID투입량
반응물Cyanogen BromideHCID 10476—
반응물Sodium AcetateHCID 517045—
반응물N2-[1-benzyl-2-(1-[(1,2-dimethylhydrazino) carbonyl]-3-methylbutylamino)-2-oxoethyl]-2-pyrazinecarboxamideHCID 67326475—
용매MethanolHCID 887—
생성물N2-[1-benzyl-2-(1-[(2-cyano-1,2-dimethylhydrazino)carbonyl]-3-methylbutylamino)-2-oxoethyl]-2-pyrazinecarboxamideHCID 8665508665%

반응 단계

N2-[1-benzyl-2-(1-[(1,2-dimethylhydrazino)carbonyl]-3-methylbutylamino)-2-oxoethyl]-2-pyrazinecarboxamide (100 mg, 0.23 mmol) and sodium acetate (53 mg, 0.64 mmol) were dissolved in methanol (1 mL). Cyanogen bromide (49 mg, 0.46 mmol) was added and the solution was stirred for 4 h. Methanol was concentrated by rotary evaporation. The pH value was adjusted (5% NaHSO3) to 1-2. The solution was extracted by EtOAc, and washed with water and brine. The organic layer was dried over Na2SO4, filtered, and concentrated by rotary evaporation. Purification by chromatography (silica, 1/1: Hexane/EtOAc, Rf=0.3) afforded N2-[1-benzyl-2-(1-[(2-cyano-1,2-dimethylhydrazino)carbonyl]-3-methylbutylamino)-2-oxoethyl]-2-pyrazinecarboxamide as pale yellow solid (67 mg, 65%).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08895497B2
출처 데이터셋uspto-grants-2014_11
ORD IDord-42bbe04e1bab4235b635b1af104f8142
출처 메모uspto-grants-2014_11