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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 230271생성일: 2026년 10월 23일

Water → (+/-)-5-(2-Methyl-propane-2-sulfinylamino)-2-(6-methyl-2-p-tolyl-imidazo[1,2-a]pyridin-3-yl)-pentanoic acid methyl ester

https://huagongshe.com/ko/reaction/230271

반응식

참여 물질

역할이름HCID투입량
반응물WaterHCID 962—
반응물Tert-ButanesulfinamideHCID 3382465—
반응물Sodium borohydrideHCID 4311764—
반응물2-(6-Methyl-2-p-tolyl-imidazo[1,2-a]pyridin-3-yl)-5-oxo-pentanoic acid methyl esterHCID 58763583—
촉매Titanium tetraethoxideHCID 76524—
용매TetrahydrofuranHCID 8028—
생성물(+/-)-5-(2-Methyl-propane-2-sulfinylamino)-2-(6-methyl-2-p-tolyl-imidazo[1,2-a]pyridin-3-yl)-pentanoic acid methyl esterHCID 58763604—

반응 단계

To a magnetically stirred solution of 2-(6-methyl-2-p-tolyl-imidazo[1,2-a]pyridin-3-yl)-5-oxo-pentanoic acid methyl ester 44a (0.066 g, 0.189 mmol) in THF (2 mL) at room temperature under Ar atmosphere was added 2-methyl-propane-2-sulfinic acid amide (0.023 g, 0.189 mmol) and titanium ethoxide (20 wt % solution in ethanol, 2 mL). The reaction mixture was stirred overnight at room temperature. Water (40 mL) was added, and the aqueous phase was extracted with ethyl acetate (2×40 mL). The combined organic layers were washed with water, dried (MgSO4), and concentrated in vacuo. The reaction mixture was redissolved in MeOH (2 mL) and sodium borohydride (0.014 mg, 0.378 mmol) was added at room temperature. The reaction mixture was stirred for 1 h at room temperature, then water (40 mL) was added, and the aqueous phase was extracted with ethyl acetate (2×100 mL). The combined organic layers were washed with water, dried (MgSO4), and concentrated in vacuo to provide crude product.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07566725B2
출처 데이터셋uspto-grants-2009_07
ORD IDord-1f0f7094ad0f49a39acdd7168a078d69
출처 메모uspto-grants-2009_07