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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 490080생성일: 2026년 10월 25일

Water → 1-Isobutyl-4-(5-nitro-pyridin-2-yl)-piperazine

https://huagongshe.com/reaction/490080

반응식

참여 물질

역할이름HCID투입량
반응물WaterHCID 962—
반응물TetrahydrofuranHCID 8028—
반응물1-(5-Nitropyridin-2-yl)piperazineHCID 2928799—
반응물Sodium triacetoxyborohydrideHCID 5049666—
용매Acetic AcidHCID 176—
생성물1-Isobutyl-4-(5-nitro-pyridin-2-yl)-piperazineHCID 68406877—

반응 단계

A mixture of 7 g (34 mmol) 1-(5-nitro-pyridin-2-yl)-piperazine (commercially available), 3.15 g (44 mmol) isobutytraldehyde, 10.7 g (50 mmol) sodium trisacetoxyborohydride in 140 ml THF and 3 ml acetic acid was stirred at room temperature for 16 h. After addition of 50 ml water, THF was removed under vacuum. The residue was taken up in 300 ml water and 400 ml ethyl acetate and made alkaline by addition of 2M aq. Na2CO3 solution. The mixture was afterwards extracted two times with 300 ml ethyl acetate each. The combined organic phases were washed two times with 200 ml water each, dried with MgSO4 and evaporated to dryness. The residue was used without further purification in the synthesis of intermediate 9. (m/e): 265.0 (MH+; 100%).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07528135B2
출처 데이터셋uspto-grants-2009_05
ORD IDord-0772e6aed8594464b169c4b07f50916d
출처 메모uspto-grants-2009_05