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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 83162생성일: 2026년 10월 23일

(5-Methyl-3-phenyl-1,2-oxazol-4-yl)methanol → 4-Benzyloxy-2-(5-methyl-3-phenyl-isoxazol-4-ylmethoxy)-pyridine

https://huagongshe.com/ko/reaction/83162

반응식

참여 물질

역할이름HCID투입량
반응물(5-Methyl-3-phenyl-1,2-oxazol-4-yl)methanolHCID 2776149—
반응물4-Benzyloxy-2(1H)-pyridoneHCID 3607724—
생성물4-Benzyloxy-2-(5-methyl-3-phenyl-isoxazol-4-ylmethoxy)-pyridineHCID 4262907128%

반응 단계

As described for example 4, (5-methyl-3-phenyl-isoxazol-4-yl)-methanol (95 mg, 0.50 mmol) was converted using 4-benzyloxy-2(1H)-pyridone instead of 2-hydroxy-5-trifluoromethylpyridine to the title compound (SiO2, heptane:ethyl acetate=95:5 to 0:100, 52 mg, 28%) which was obtained as a colourless oil. MS: m/e=373.1 [M+H]+.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08846719B2
출처 데이터셋uspto-grants-2014_09
ORD IDord-2025ce0193bb489ba038c8fe32c132c4
출처 메모uspto-grants-2014_09