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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 11720생성일: 2026년 10월 23일

Acetic Acid → (5-Chloro-2-{2-[4-(4-fluoro-benzyl)-(2R,5S)-2,5-dimethyl-piperazin-1-yl]-2-oxo-ethoxy}-pyridin-3-ylamino)-acetic Acid Ethyl Ester

https://huagongshe.com/ko/reaction/11720

반응식

참여 물질

역할이름HCID투입량
반응물Acetic AcidHCID 176—
반응물Ethyl oxoacetateHCID 70211—
반응물Sodium cyanoborohydrideHCID 5003444—
반응물Sodium triacetoxyborohydrideHCID 5049666—
반응물2-(3-Amino-5-chloro-pyridin-2-yloxy)-1-[4-(4-fluoro-benzyl)-(2R,5S)-2,5-dimethyl-piperazin-1-yl]-ethanoneHCID 69655590—
용매1,2-DichloroethaneHCID 11—
용매WaterHCID 962—
생성물(5-Chloro-2-{2-[4-(4-fluoro-benzyl)-(2R,5S)-2,5-dimethyl-piperazin-1-yl]-2-oxo-ethoxy}-pyridin-3-ylamino)-acetic Acid Ethyl EsterHCID 6965541066.3%

반응 단계

To a solution of 2-(3-amino-5-chloro-pyridin-2-yloxy)-1-[4-(4-fluoro-benzyl)-(2R,5S)-2,5-dimethyl-piperazin-1-yl]-ethanone (0.105 g, 0.26 mmol) in 1,2-dichloroethane (2 mL) was added ethyl glyoxylate (0.050 mL, ˜0.5 mmol, 50% solution in toluene), acetic acid (0.016 mL, 0.28 mmol) and sodium triacetoxyborohydride (0.085 g, 0.40 mmol). The reaction was stirred at ambient temperature for 18 hours. Additional ethyl glyoxylate (0.050 mL, ˜0.5 mmol, 50% solution in toluene) and acetic acid (0.016 mL, 0.28 mmol) were added and the reaction was warmed to reflux for 3 hours. The reaction was then cooled to ambient temperature, sodium cyanoborohydride (˜0.030 g, 0.48 mmol) was added and the reaction was stirred at ambient temperature for 18 hours. The reaction was diluted with water and extracted with methylene chloride. The organic layer was dried over magnesium sulfate, filtered and concentrated in vacuo. Flash chromatography on silica gel provided the title compound (0.085 g).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07098212B2
출처 데이터셋uspto-grants-2006_08
ORD IDord-f0f58e90bcac4453b21715f59bac8cc4
출처 메모uspto-grants-2006_08