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HRID 1254703作成日:2026年10月26日

Citric Acid → (2r,3s)-2-(4-Cyano-2-methyl-3-(trifluoromethyl)phenylamino)-3-hydroxybutanoic acid

https://huagongshe.com/reaction/1254703

反応式

関与物質

役割名称HCID仕込み量
反応物Citric AcidHCID 311—
反応物Potassium CarbonateHCID 11430—
反応物D-ThyronineHCID 6951212—
反応物4-Fluoro-3-methyl-2-(trifluoromethyl)benzonitrileHCID 66624938—
溶媒Dimethyl SulfoxideHCID 679—
生成物(2r,3s)-2-(4-Cyano-2-methyl-3-(trifluoromethyl)phenylamino)-3-hydroxybutanoic acidHCID 6698093726.9%

反応条件

温度75 °C

反応手順

4-fluoro-3-methyl-2-(trifluoromethyl)benzonitrile (1.0 g, 4.92 mmol) and D-theronine (703 mg, 90 mmol) were added to DMSO (15 mL). K2CO3 (3.26 g) was added to the reaction mixture and stirred at 75° C. for 24 h. The reaction mixture was cooled to room temperature and poured slowly in to a 10% citric acid solution and stirred for 10 min at room temperature. The solution was extracted with EtOAc several times to give the crude product. The crude product was chromatographed with a gradient of hexanes/EtOAc and then with EtOAc, 100% to give the final product (400 mg). 1H NMR (500 MHz, acetone-d6, δ in ppm) 7.62 (d, J=9 Hz, 1H), 6.98 (d, J=9 Hz, 1H), 5.52 (d, J=9 Hz, 1H), 4.52 (m, 1H), 4.32 (m, 1H), 2.35 (s, 3H), 1.35 (d, J=6 Hz, 3H).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08455525B2
出典データセットuspto-grants-2013_06
ORD IDord-daca09fcf85c4db8b583f3b6b21b2510
出典メモuspto-grants-2013_06