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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 77318생성일: 2026년 10월 26일

Water → N-isoamyl-N-(6-acetoxy naphthalene-2-sulfonyl)-D-valine tert-butyl ester

https://huagongshe.com/reaction/77318

반응식

참여 물질

역할이름HCID투입량
반응물WaterHCID 962—
반응물1-Bromo-3-methylbutaneHCID 7891—
반응물Potassium CarbonateHCID 11430—
반응물N-(6-acetoxy naphthalene-2-sulfonyl)-D-valine tert-butyl esterHCID 67155170—
용매DimethylformamideHCID 6228—
생성물N-isoamyl-N-(6-acetoxy naphthalene-2-sulfonyl)-D-valine tert-butyl esterHCID 6715527268%

반응 단계

To a solution of N-(6-acetoxy naphthalene-2-sulfonyl)-D-valine tert-butyl ester (3.15 g, 7.48 mmol) in N,N-dimethylformamide (15 mL) is added potassium carbonate (3.09 g, 22.36 mmol), followed by 1-bromo-3-methyl butane (1.79 mL, 14.94 mmol), and the reaction is allowed to stir at ambient temperature for 16 h. Another equivalent of 1-bromo-3-methyl butane (0.9 mL, 7.5 mmol) is added and the reaction is allowed to stir for 16 h at ambient temperature. The reaction is poured over water and extracted three times with dichloromethane. The combined organic extracts are washed with brine, dried over magnesium sulfate and concentrated in vacuo. The crude product is purified by column chromatography and eluted with a gradient of 2-7% (hexanes-ethyl acetate) to afford the title compound as a yellow oil (2.5 g, 68% yield), along with N-isoamyl-N-(6-(3-methylbutoxy)naphthalene-2-sulfonyl)-D-valine tert-butyl ester as a yellow oil (0.3 g, 7.7% yield). LCMS (m/z): (492.26; M+1).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08841291B2
출처 데이터셋uspto-grants-2014_09
ORD IDord-4536dfcebac34c8ea9fe3b69ded015d4
출처 메모uspto-grants-2014_09