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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 538417생성일: 2026년 10월 26일

Sodium Carbonate → 5-(2-(4-Fluorophenyl)oxazol-4-yl)-3-methoxypyridin-2-amine

https://huagongshe.com/reaction/538417

반응식

참여 물질

역할이름HCID투입량
반응물Sodium CarbonateHCID 10340—
반응물2-(4-Fluorophenyl)oxazol-4-yl trifluoromethanesulfonateHCID 11659599—
반응물3-Methoxy-5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)pyridin-2-amineHCID 53398059—
용매WaterHCID 962—
용매1,2-DimethoxyethaneHCID 8071—
생성물5-(2-(4-Fluorophenyl)oxazol-4-yl)-3-methoxypyridin-2-amineHCID 6659053963.5%

반응 단계

A mixture of 3-methoxy-5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)pyridin-2-amine (200 mg, 0.8 mmol) and 2-(4-fluorophenyl)oxazol-4-yl trifluoromethanesulfonate (250 mg, 0.8 mmol), and 2.0 M aqueous Na2CO3 (1.2 mL, 2.4 mmol) in DME (2.0 mL) was sparged with Ar. Dichlorobis(triphenylphosphine)palladium(0) (281 mg, 0.4 mmol) was added and the reaction mixture was irradiated at 150° C. for 15 min in a microwave reactor. After cooling to rt, the reaction mixture was diluted with water and extracted with EtOAc (3×). The combined organic layers were dried over sodium sulfate, filtered and concentrated in vacuo. The residue was purified by flash chromatography over (SiO2, 100:0-0:100 hexanes-EtOAc) to provide 145 mg of 5-(2-(4-fluorophenyl)oxazol-4-yl)-3-methoxypyridin-2-amine: LCMS (m/z): 286.1 (MH+), tR=0.68 min.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08865732B2
출처 데이터셋uspto-grants-2014_10
ORD IDord-87b09bd64e504677ad35b4828e23f357
출처 메모uspto-grants-2014_10