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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1066495생성일: 2026년 10월 26일

Ethanol → 5-Methyl-pyridine-2-sulfonic acid [2-(3-hydroxy-phenyl)-6-methoxy-5-(2-methoxy-phenoxy)-pyrimidin-4-yl]-amide

https://huagongshe.com/reaction/1066495

반응식

참여 물질

역할이름HCID투입량
반응물EthanolHCID 702—
반응물1,3-CyclohexadieneHCID 11605—
반응물5-Methyl-pyridine-2-sulfonic acid [2-(3-benzyloxy-phenyl)-6-methoxy-5-(2-methoxy-phenoxy)-pyrimidin-4-yl]-amideHCID 53801719—
촉매PalladiumHCID 23938—
용매1,4-DioxaneHCID 31275—
생성물5-Methyl-pyridine-2-sulfonic acid [2-(3-hydroxy-phenyl)-6-methoxy-5-(2-methoxy-phenoxy)-pyrimidin-4-yl]-amideHCID 9848584—

반응 단계

1.46 g of 5-methyl-pyridine-2-sulfonic acid [2-(3-benzyloxy-phenyl)-6-methoxy-5-(2-methoxy-phenoxy)-pyrimidin-4-yl]-amide were dissolved in dioxane (25 ml) by gentle warming than ethanol (50 ml) was added followed by cyclohexadiene (6 g) and palladium on charcoal, 10%, (1.46 g). The solution was refluxed for 20 h, the catalyst removed by filtration and the solution concentrated on a rotary evaporator. The yellow crystalline solid that precipitated was collected, washed with ether and dried in a vacuum to give the desired 5-methyl-pyridine-2-sulfonic acid [2-(3-hydroxy-phenyl)-6-methoxy-5-(2-methoxy-phenoxy)-pyrimidin-4-yl]-amide as off-white crystals. ISP mass spectrum, m/e 495.2 (M+1 calculated for C24H22N4O6S1: 495). Melting point 211°-216° C.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06242601B1
출처 데이터셋uspto-grants-2001_06
ORD IDord-d4d00f622d1a4fadaad775f5f73fa339
출처 메모uspto-grants-2001_06