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HRID 1984640作成日:2026年10月25日

Triethylamine → 2-(5-Methyl-3-phenyl-isoxazol-4-ylethynyl)-pyridine

https://huagongshe.com/reaction/1984640

反応式

関与物質

役割名称HCID仕込み量
反応物TriethylamineHCID 8471—
反応物1,3-Bis(diphenylphosphino)propaneHCID 81219—
反応物EthynylpyridineHCID 137268—
反応物4-Iodo-5-methyl-3-phenylisoxazoleHCID 2776150—
触媒palladium(II) acetateHCID 167845—
溶媒DimethylformamideHCID 6228—
生成物2-(5-Methyl-3-phenyl-isoxazol-4-ylethynyl)-pyridineHCID 2478444623.1%

反応条件

温度90 °C

反応手順

A mixture of 4-iodo-5-methyl-3-phenylisoxazole (285 mg, 1.00 mmol), palladium(II) acetate (7 mg, 0.03 mmol), 1,3-bis(diphenylphosphino)propane (12 mg, 0.03 mmol), triethylamine (348 μL, 2.50 mmol) and 2-ethynylpyridine (131 μL, 1.30 mmol) in N,N-dimethylformamide (2 mL) was evaporated and flushed with argon. Cuprous iodide (4 mg, 0.02 mmol) was added and the reaction mixture was stirred for 3 h at 90° C. before cooling to ambient temperature and separated between aqueous sodium hydroxide (1 M, 30 mL) and ethyl acetate (50 mL). The aqueous layer was extracted with ethyl acetate (50 mL) and washed with aqueous sodium hydroxide (1 M, 30 mL). The combined organic layers were dried over sodium sulfate and concentrated. Purification by chromatography (SiO2, heptane:ethyl acetate=100:0 to 67:33) afforded the title compound (60 mg, 23%) as a light brown solid. MS: m/e=261.2 [M+H]+.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07544704B2
出典データセットuspto-grants-2009_06
ORD IDord-cfb5c6edebff49b29fea7c3ae5467541
出典メモuspto-grants-2009_06