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HRID 2176732作成日:2026年10月26日

Nordihydroguaretic acid → 1,4-bis{3,4-bis(2-methyl-thiazol-4-yl-methoxy)phenyl}-2,3-dimethyl-(2R,3S)-butane

https://huagongshe.com/reaction/2176732

反応式

関与物質

役割名称HCID仕込み量
反応物Nordihydroguaretic acidHCID 4534—
反応物Sodium hydrideHCID 24758—
反応物Ammonium ChlorideHCID 25517—
反応物4-(Chloromethyl)-2-methyl-1,3-thiazoleHCID 736341—
溶媒Diethyl EtherHCID 3283—
溶媒DimethylformamideHCID 6228—
生成物1,4-bis{3,4-bis(2-methyl-thiazol-4-yl-methoxy)phenyl}-2,3-dimethyl-(2R,3S)-butaneHCID 5915987542.09%

反応条件

温度0 °C

反応手順

To an ice-cooled solution of NDGA (1.50 g, 4.96 mol) in DMF (50 mL) was added 60% suspension of sodium hydride in paraffin (1.98 g=1.19 g NaH, 49.6 mmol, 10 mole equiv.). The mixture was stirred at 0° C. for 30 min. and at room temperature for 30 min. Then a solution of 4-chloromethyl-2-methylthiazole (5.86 g, 39.69 mmol, 8.0 mole equiv.) in DMF (20 mL) was added and the reaction mixture was allowed to stir for 16 h at room temperature. The reaction mixture was added to the saturated aqueous ammonium chloride (300 mL) and ether (600 mL). After shaking, the organic layer was separated, and the aqueous layer was extracted with ether (2×200 mL). The combined organic layer and extracts were washed with water (100 mL), brine (100 mL), and dried over anhydrous sodium sulfate and concentrated to dryness under reduced vacuum (30-40 mm Hg) at 25° C. The residue was dissolved in a minimum amount of dichloromethane and purified by silica gel flash chromatographic column using hexane:ethyl acetate (50:50 to 0:100) as eluant to give expected product as white solid (1.56 g, 42.09% yield). It was further purified by crystallization from acetate-hexane.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US09067875B2
出典データセットuspto-grants-2015_06
ORD IDord-d07ff72daf5a4ff19483043f85284492
出典メモuspto-grants-2015_06