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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 348441생성일: 2026년 10월 24일

1,8-Diazabicyclo(5.4.0)undec-7-ene → [5-(4-Fluorophenylcarbamoyl)pyrimidin-2-yloxy]acetic acid benzyl ester

https://huagongshe.com/ko/reaction/348441

반응식

참여 물질

역할이름HCID투입량
반응물1,8-Diazabicyclo(5.4.0)undec-7-eneHCID 81184—
반응물Benzyl 2-hydroxyacetateHCID 561337—
반응물Potassium tert-butoxideHCID 23665647—
반응물2-Methanesulfinylpyrimidine-5-carboxylic acid (4-fluorophenyl)amideHCID 86760384—
용매TetrahydrofuranHCID 8028—
용매Ethyl acetate hexaneHCID 21226206—
생성물[5-(4-Fluorophenylcarbamoyl)pyrimidin-2-yloxy]acetic acid benzyl esterHCID 1600480030.2%

반응 단계

To a solution of 2-methanesulfinylpyrimidine-5-carboxylic acid (4-fluorophenyl)amide (173 mg, contaminated with 10% sulfone, 0.62 mmol) in THF (6 mL) was added benzyl glycolate (128 μL, 0.90 mmol) followed by potassium tert-butoxide (1 M in THF, 0.3 mL, 0.3 mmol) and DBU (139 μL, 0.93 mmol). The solution was stirred for 5 h, diluted with 50% ethyl acetate/hexane, and passed through a plug of SiO2 followed by washing with 40% ethyl acetate/hexane. The filtrate was concentrated in vacuo, and the residue flash-chromatographed on SiO2 with 35% ethyl acetate/hexane to afford 71.5 mg (30% yield) of the titled product as a white solid. ESI-MS m/z 382 (MH+), 380 (M−H)−.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07176310B1
출처 데이터셋uspto-grants-2007_02
ORD IDord-7ec0e26be06e4a9b84a8b8362dc49978
출처 메모uspto-grants-2007_02