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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 2252722생성일: 2026년 10월 27일

Citric Acid → Ethanesulfonic acid {6-[2-(5-bromo-pyrimidin-2-yloxy)-ethoxy]-5-p-tolyl-pyrimidin-4-yl}-amide

https://huagongshe.com/reaction/2252722

반응식

참여 물질

역할이름HCID투입량
반응물Citric AcidHCID 311—
반응물Sodium hydrideHCID 24758—
반응물5-Bromo-2-chloropyrimidineHCID 606665—
반응물Ethanesulfonic acid [6-(2-hydroxy-ethoxy)-5-p-tolyl-pyrimidin-4-yl]-amideHCID 59645277—
용매TetrahydrofuranHCID 8028—
생성물Ethanesulfonic acid {6-[2-(5-bromo-pyrimidin-2-yloxy)-ethoxy]-5-p-tolyl-pyrimidin-4-yl}-amideHCID 1031122634.4%

반응 조건

온도50 °C

반응 단계

Ethanesulfonic acid [6-(2-hydroxy-ethoxy)-5-p-tolyl-pyrimidin-4-yl]-amide (135 mg) was dissolved in THF (15 ml) and sodium hydride (80 mg) was added followed by stirring for 15 min at 50° C. Then 2-chloro-5-bromo-pyrimidine (162 mg) was added and stirring was continued for 8 h at 70 C. The reaction mixture was poured onto ice water, acidified with solid citric acid and extracted with ethylacetate. The combined organic extracts were dried over magnesium sulfate and the solvent was evaporated. The crude material was purified by plate chromatography with ethyl acetate/hexane=½ to give ethanesulfonic acid {6-[2-(5-bromo-pyrimidin-2-yloxy)-ethoxy]-5-p-tolyl-pyrimidin-4-yl}-amide (68 mg) as a white powder. LC-MS: tR: 4.64, [M+H]+: 496.19.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07323465B2
출처 데이터셋uspto-grants-2008_01
ORD IDord-655d6fd4792649d384053cec1d355535
출처 메모uspto-grants-2008_01