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HRID 1885195作成日:2026年10月25日

2-Chloro-1,3-oxazole → 4-Acetoxy-3,5-dimethoxycinnamic acid chloride

https://huagongshe.com/reaction/1885195

反応式

関与物質

役割名称HCID仕込み量
反応物2-Chloro-1,3-oxazoleHCID 13371074—
反応物3-[4-(Acetyloxy)-3,5-dimethoxyphenyl]prop-2-enoic acidHCID 53661480—
触媒DimethylformamideHCID 6228—
溶媒TetrahydrofuranHCID 8028—
生成物4-Acetoxy-3,5-dimethoxycinnamic acid chlorideHCID 54113742—

反応手順

To a mixture o 4-acetoxy-3,5-dimethoxycinnamic acid (638 mg), dimethylformamide (2 drops) and tetrahydrofuran (8 ml) was added oxazolyl chloride (0.25 ml). The mixture was stirred at room temperature for one hour and then the solvent was distilled off to obtain 4-acetoxy-3,5-dimethoxycinnamic acid chloride as crystals. To a solution of the crystals in dichloromethane (15 ml) were added 5-amino-4-(2-chlorophenyl)-2-ethylthieno[2,3-b]pyridine (576 mg) and N,N-dimethylaniline (0.25 ml) with ice cooling. After warming to room temperature, the mixture was stirred for 5 hours, washed in turn with water, aqueous saturated NaHCO3 solution and water, and then dried over MgSO4. The solvent was distilled off and the residue was crystallized from ethanol (729 mg, 67.4%). 5-(4-Acetoxy-3,5-dimethoxycinnamoylamino)-4-(2-chloropheny ethylthieno[2,3-b]pyridine was obtained as colorless prisms by recrystallization from acetone, mp: 133°-135° C.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05143919
出典データセットuspto-grants-1992_09
ORD IDord-b5bcc80e822d40a4b6cf41b1a112af29
出典メモuspto-grants-1992_09