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HRID 1254656作成日:2026年10月25日

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

https://huagongshe.com/reaction/1254656

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-ThreonineHCID 69435—
反応物4-Fluoro-2-(trifluoromethyl)benzonitrileHCID 605085—
溶媒Dimethyl SulfoxideHCID 679—
生成物(2r,3s)-2-(4-Cyano-3-(trifluoromethyl)phenylamino)-3-hydroxybutanoic acidHCID 6700626255.6%

反応条件

温度75 °C

反応手順

4-fluoro-2-(trifluoromethyl)benzonitrile (194853-86-6) (2.0 g, 10.6 mmol) was mixed together with H-D-Thr-OH (1.51 g, 12.69 mmol) in DMSO (30 mL). K2CO3 (3.06 g, 22.21 mmol) 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 into a 10% citric acid solution and stirred for 10 min at room temperature. The solution was extracted with EtOAc several times to get the crude product. The crude product was chromatographed with a gradient of hexanes/EtOAc and then with EtOAc, 100% to get the pure final product (1.7 g): 1H NMR (500 MHz, CDCl3, δ in ppm) 9.02 (br s, 1H), 7.76 (d, J=9 Hz, 1H), 7.52 (s, 1H), 7.39 (d, J=9 Hz, 1H), 6.41d, J=9 Hz, 1H), 4.42 (m, 1H), 4.01 (m, 1H), 1.24 (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-dde60e39eaf249c98dbc415d515109c8
出典メモuspto-grants-2013_06