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HRID 563202作成日:2026年10月25日

Citric Acid → (2r,3s)-2-(4-Cyanonaphthalen-1-ylamino)-3-hydroxybutanoic acid

https://huagongshe.com/reaction/563202

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1-Cyano-4-fluoronaphthaleneHCID 2736734—
溶媒Dimethyl SulfoxideHCID 679—
生成物(2r,3s)-2-(4-Cyanonaphthalen-1-ylamino)-3-hydroxybutanoic acidHCID 6700657269.7%

反応条件

温度75 °C

反応手順

4-fluoro-1-naphthonitrile (13916-99-9) (1.0 g, 5.84 mmol) was mixed together with H-D-Thr-OH (835 mg, 7.01 mmol) in DMSO (20 mL). K2CO3 (1.61 g, 11.68 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 hexane/EtOAc and then with EtOAc, 100% to get the pure final product (1.1 g): 1H NMR (500 MHz, acetone-d6, δ in ppm) 8.25 (d, J=9 Hz, 1H), 8.09 (d, J=9 Hz, 1H), 7.84 (d, J=9 Hz, 1H), 7.75 (t, J=9 Hz, 1H), 7.65 (t, J=9 Hz, 1H), 6.70 (d, J=9 Hz, 1H), 6.32 (d, J=9 Hz, 1H), 4.53 (m, 1H), 4.38 (m, 1H), 1.40 (d, J=6 Hz, 3H).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08067448B2
出典データセットuspto-grants-2011_11
ORD IDord-ae6e592f384d43e083b7ccdc203e0053
出典メモuspto-grants-2011_11