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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 2252735생성일: 2026년 10월 27일

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

https://huagongshe.com/reaction/2252735

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참여 물질

역할이름HCID투입량
반응물Citric AcidHCID 311—
반응물Sodium hydrideHCID 24758—
반응물2-Chloro-5-methoxypyrimidineHCID 589058—
반응물Ethanesulfonic acid [6-(2-hydroxy-ethoxy)-5-(2-methoxy-phenoxy)-[2,2]bipyrimidinyl-4-yl]-amideHCID 59645268—
용매TetrahydrofuranHCID 8028—
생성물Ethanesulfonic acid [6-[2-(5-methoxy-pyrimidin-2-yloxy)-ethoxy]-5-(2-methoxy-phenoxy)-[2,2']bipyrimidinyl-4-yl]-amideHCID 5964526955.2%

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 (6 ml). Sodium hydride (40 mg) and 2-chloro-5-methoxy-pyrimidine (92 mg) were added and the mixture was heated to 75° C. for 46 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-methoxy-pyrimidin-2-yloxy)-ethoxy]-5-(2-methoxy-phenoxy)-[2,2′]bipyrimidinyl-4-yl]-amide (61 mg) as a white powder. LC-MS: tR: 3.87, [M−H]+: 554.02.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07323465B2
출처 데이터셋uspto-grants-2008_01
ORD IDord-8138d20e24d94332a8035fd61bd7b0ff
출처 메모uspto-grants-2008_01