戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 83112作成日:2026年10月26日

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

https://huagongshe.com/reaction/83112

反応式

関与物質

役割名称HCID仕込み量
反応物N,N,N',N'-TetramethylazodicarboxamideHCID 4278—
反応物TriphenylphosphineHCID 11776—
反応物TributylphosphineHCID 13831—
反応物ethyl N-ethoxycarbonyliminocarbamateHCID 220568—
反応物(5-Methyl-3-phenyl-1,2-oxazol-4-yl)methanolHCID 2776149—
反応物HCID 178516071HCID 178516071—
溶媒TetrahydrofuranHCID 8028—
生成物2-(5-Methyl-3-phenyl-isoxazol-4-ylmethoxy)-pyridineHCID 6844468525.5%

反応条件

温度0 °C

反応手順

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]+.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08846719B2
出典データセットuspto-grants-2014_09
ORD IDord-0676116bc51c4e2380abddac05371dec
出典メモuspto-grants-2014_09