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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 83112생성일: 2026년 10월 25일

N,N,N',N'-Tetramethylazodicarboxamide → 2-(5-Methyl-3-phenyl-isoxazol-4-ylmethoxy)-pyridine

https://huagongshe.com/reaction/83112

반응식

참여 물질

역할이름HCID투입량
반응물N,N,N',N'-TetramethylazodicarboxamideHCID 4278—
반응물TriphenylphosphineHCID 11776—
반응물TributylphosphineHCID 13831—
반응물ethyl N-ethoxycarbonyliminocarbamateHCID 220568—
반응물(5-Methyl-3-phenyl-1,2-oxazol-4-yl)methanolHCID 2776149—
반응물HCID 178516071HCID 178516071—
용매TetrahydrofuranHCID 8028—
생성물2-(5-Methyl-3-phenyl-isoxazol-4-ylmethoxy)-pyridineHCID 6844468525.5%

반응 조건

온도0 °C

반응 단계

To a solution of (5-methyl-3-phenyl-isoxazol-4-yl)-methanol (100 mg, 0.53 mmol) in THF (6 mL) was added 2-hydroxypyridine (50 mg, 0.53 mmol) and tributyl phosphine (206 μL, 0.79 mmol) at ambient temperature under an argon atmosphere. After cooling to 0° C., N,N,N′,N′-tetramethylazodicarboxamide (137 mg, 0.79 mmol) was added. The resulting orange solution was stirred for 16 h at ambient temperature followed by 2.5 h at 50° C. Then triphenylphosphine (208 mg, 0.79 mmol), 2-hydroxypyridine (50 mg, 0.53 mmol) and diethyl azodicarboxylate (127 μL, 0.79 mmol) were added and the reaction mixture was stirred for 4 h at 50° C. The reaction mixture was then evaporated. Purification by chromatography (SiO2, heptane:ethyl acetate=95:5 to 0:100) afforded the title compound (36 mg, 25%) as a colourless oil. MS: m/e=267.2 [M+H]+.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08846719B2
출처 데이터셋uspto-grants-2014_09
ORD IDord-0676116bc51c4e2380abddac05371dec
출처 메모uspto-grants-2014_09