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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1014872생성일: 2026년 10월 24일

Ethyl Acetate → 3-((R)-2-(methoxymethyl)pyrrolidine-1-carbonyl)-5-(oxazol-2-yl)benzoic acid

https://huagongshe.com/reaction/1014872

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참여 물질

역할이름HCID투입량
반응물Ethyl AcetateHCID 8857—
반응물2-(Tri-n-butylstannyl)oxazoleHCID 15486183—
반응물(R)-methyl 3-bromo-5-(2-(methoxymethyl)pyrrolidine-1-carbonyl)benzoateHCID 67315972—
촉매HCID 178418397HCID 178418397—
용매1,4-DioxaneHCID 31275—
생성물3-((R)-2-(methoxymethyl)pyrrolidine-1-carbonyl)-5-(oxazol-2-yl)benzoic acidHCID 5934684975.7%

반응 조건

온도95 °C

반응 단계

To a solution of (R)-methyl 3-bromo-5-(2-(methoxymethyl)pyrrolidine-1-carbonyl)benzoate (Step H (1), 350 mg, 1.0 mmol) in dioxane (5 mL) were added Pd(PPh3)4 (173.5 mg, 0.15 mmol) and 2-(tributylstannyl)oxazole (1.8 g, 5.0 mmol) above made and the reaction mixture was stirred at 95° C. with sealed cap for 16 h. Ethyl acetate (200 mL) was added and the mixture was washed with H2O and concentrated under vacuum. The crude mixture was purified by silica gel Flash Chromatography (0% to 30% to 50% to 70% EtOAc/Hexane step gradient) to give 250 mg of the title compound: 1H NMR (CDCl3, 500 MHz) δ ppm 1.75-2.11 (4H, m), 3.08 (1H, brd s), 3.38 (3H, s), 3.50 (1H, m), 3.63 (2H, s), 3.83 (3H, s), 4.43 (1H, s), 7.24 (1H, s), 7.73 (1H, s), 8.22 (1H, s), 8.35 (1H, s), 8.71 (1H, s). MS (ESI) (M+H)+ 345.26.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07981913B2
출처 데이터셋uspto-grants-2011_07
ORD IDord-458decd3ac8a427b856a65e5d7091027
출처 메모uspto-grants-2011_07