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HRID 274241생성일: 2026년 10월 25일

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

https://huagongshe.com/reaction/274241

반응식

참여 물질

역할이름HCID투입량
반응물WaterHCID 962—
반응물Tert-butoxycarbonylalanineHCID 85082—
반응물1,3-Propanediamine, N'-(ethylcarbonimidoyl)-N,N-dimethyl-, monohydrochlorideHCID 2723939—
반응물Ethyl 2-(2-Amino-4-thiazolyl)-2-oxoacetateHCID 4356513—
촉매4-(Dimethylamino)pyridineHCID 14284—
용매DimethylformamideHCID 6228—
생성물ethyl 2-[2-(Boc-L-alanyl)aminothiazol-4-yl]glyoxylateHCID 1865916171.4%

반응 단계

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.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05389625
출처 데이터셋uspto-grants-1995_02
ORD IDord-f36417eb0f2945ac991ee10e1df38efd
출처 메모uspto-grants-1995_02