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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 2252729생성일: 2026년 10월 27일

Citric Acid → Ethanesulfonic acid [6-[2-(5-bromo-pyrimidin-2-yloxy)-ethoxy]-5-(2-methoxy-phenoxy)-[2,2']bipyrimidinyl-4-yl]-amide

https://huagongshe.com/reaction/2252729

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참여 물질

역할이름HCID투입량
반응물Citric AcidHCID 311—
반응물Sodium hydrideHCID 24758—
반응물5-Bromo-2-chloropyrimidineHCID 606665—
반응물Ethanesulfonic acid [6-(2-hydroxy-ethoxy)-5-(2-methoxy-phenoxy)-[2,2]bipyrimidinyl-4-yl]-amideHCID 59645268—
용매TetrahydrofuranHCID 8028—
생성물Ethanesulfonic acid [6-[2-(5-bromo-pyrimidin-2-yloxy)-ethoxy]-5-(2-methoxy-phenoxy)-[2,2']bipyrimidinyl-4-yl]-amideHCID 1024009344.9%

반응 조건

온도75 °C

반응 단계

Ethanesulfonic acid [6-(2-hydroxy-ethoxy)-5-(2-methoxy-phenoxy)-[2,2]bipyrimidinyl-4-yl]-amide (89 mg) was dissolved in THF (10 ml). Sodium hydride (60 mg) and 2-chloro-5-bromo-pyrimidine (100 mg) were added and the mixture was heated to 75° C. for 48 h, then poured onto water, acidified with solid citric acid and the precipitate was filtered off. The crude material was purified by crystallization from methanol to give ethanesulfonic acid [6-[2-(5-bromo-pyrimidin-2-yloxy)-ethoxy]-5-(2-methoxy-phenoxy)-[2,2′]bipyrimidinyl-4-yl]-amide (54 mg) as a white powder. LC-MS: tR: 4.23, [M+H]+: 605.90.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07323465B2
출처 데이터셋uspto-grants-2008_01
ORD IDord-a89081a8a3864250a685fe7912b922a2
출처 메모uspto-grants-2008_01