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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 2252728생성일: 2026년 10월 25일

1,2-Dimethoxyethane → Ethanesulfonic acid [6-(2-hydroxy-ethoxy)-5-(2-methoxy-phenoxy)-[2,2]bipyrimidinyl-4-yl]-amide

https://huagongshe.com/reaction/2252728

반응식

참여 물질

역할이름HCID투입량
반응물1,2-DimethoxyethaneHCID 8071—
반응물Potassium tert-butoxideHCID 23665647—
반응물Ethanesulfonic acid [6-chloro-5-(2-methoxy-phenoxy)-[2,2']bipyrimidinyl-4-yl]-amideHCID 59645271—
용매Ethylene GlycolHCID 174—
생성물Ethanesulfonic acid [6-(2-hydroxy-ethoxy)-5-(2-methoxy-phenoxy)-[2,2]bipyrimidinyl-4-yl]-amideHCID 59645268—

반응 조건

온도85 °C

반응 단계

To a solution of potassium tert.-butoxide (366.5 mg) in ethylene glycol (5 ml) was added 1,2-dimethoxy ethane (5 ml) and ethanesulfonic acid [6-chloro-5-(2-methoxy-phenoxy)-[2,2′]bipyrimidinyl-4-yl]-amide (420 mg). The reaction mixture was heated to 85° C. for 7 days, concentrated in vacuo, poured onto water, acidified by 2N HCl, and extracted with ethyl acetate. The combined organic extracts were dried over magnesium sulfate and concentrated in vacuo. The precipitated product was washed with diethyl ether, filtered and dried at HV to give ethanesulfonic acid [6-(2-hydroxy-ethoxy)-5-(2-methoxy-phenoxy)-[2,2′]bipyrimidinyl-4-yl]-amide (400 mg). LC-MS: tR: 3.45, [M+H]+: 448.24.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07323465B2
출처 데이터셋uspto-grants-2008_01
ORD IDord-daca05c35a284770ab324c5d6ee82d46
출처 메모uspto-grants-2008_01