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HRID 274241作成日:2026年10月26日

Water → ethyl 2-[2-(Boc-L-alanyl)aminothiazol-4-yl]glyoxylate

https://huagongshe.com/reaction/274241

反応式

関与物質

役割名称HCID仕込み量
反応物WaterHCID 962—
反応物Tert-butoxycarbonylalanineHCID 85082—
反応物1,3-Propanediamine, N'-(ethylcarbonimidoyl)-N,N-dimethyl-, monohydrochlorideHCID 2723939—
反応物Ethyl 2-(2-Amino-4-thiazolyl)-2-oxoacetateHCID 4356513—
触媒4-(Dimethylamino)pyridineHCID 14284—
溶媒DimethylformamideHCID 6228—
生成物ethyl 2-[2-(Boc-L-alanyl)aminothiazol-4-yl]glyoxylateHCID 1865916171.4%

反応手順

Ethyl 2-(2-aminothiazol-4-yl)glyoxylate (4.0 g) and Boc-L-alanine (5.67 g) were dissolved in 40 ml of N,N-dimethylformamide (hereafter abbreviated as DMF), and thereto was added 1-ethyl-3-(3'-dimethylaminopropyl)carbodiimide hydrochloride (5.74 g) under ice-cooling followed by addition of 4-dimethylaminopyridine (0.4 g). The mixture was stirred at room temperature for 5 hours. Water (400 ml) was added thereto, and the mixture was extracted twice with ethyl acetate (300 ml). The ethyl acetate layer was washed with 10% aqueous solution of citric acid (200 ml), saturated aqueous solution of sodium bicarbonate (200 ml) and saturated brine (200 ml) in this order, and dried over anhydrous sodium sulfate. The ethyl acetate was distilled off under reduced pressure, and the residue was subjected to silica gel column chromatography eluted with benzene-ethyl acetate. The object fraction was concentrated to give 5.30 g of ethyl 2-[2-(Boc-L-alanyl)aminothiazol-4-yl]glyoxylate.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05389625
出典データセットuspto-grants-1995_02
ORD IDord-f36417eb0f2945ac991ee10e1df38efd
出典メモuspto-grants-1995_02