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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 470812생성일: 2026년 10월 26일

Potassium Carbonate → (2R,3R)-2-(3-Chloro-4-cyanophenylamino)-3-hydroxybutanoic acid

https://huagongshe.com/reaction/470812

반응식

참여 물질

역할이름HCID투입량
반응물Potassium CarbonateHCID 11430—
반응물D-AllothreonineHCID 90624—
반응물2-Chloro-4-fluorobenzonitrileHCID 109000—
용매Dimethyl SulfoxideHCID 679—
생성물(2R,3R)-2-(3-Chloro-4-cyanophenylamino)-3-hydroxybutanoic acidHCID 67006815100%

반응 조건

온도75 °C

반응 단계

To a suspension of D-allo-threonine (5.08 g, 42.7 mmol) and K2CO3 (10.32 g, 74.7 mmol) in DMSO (50 mL) was added 2-chloro-4-fluorobenzonitrile (5.53 g, 35.5 mmol) at room temperature. The reaction mixture was heated to 75° C. and stirred for 39 h. The reaction mixture was allowed to cool to room temperature and quenched with H2O (400 mL) and extracted with EtOAc (3×200 mL). The aqueous layer was then acidified with solid citric acid and extracted with EtOAc (2×100 mL). The later organic extracts were combined, washed with H2O (3×150 mL), dried (Na2SO4), filtered and concentrated under reduced pressure to provided the title compound as a brown solid (9.04 g, 100%): 1H NMR (400 MHz, acetone-d6, δ in ppm) 7.51 (d, J=8.8 Hz, 1H), 6.97 (d, J=2.3 Hz, 1H), 6.83 (dd, J=2.4, 8.8 Hz, 1H), 6.31 (br d, J=7.6 Hz, 1H), 4.28-4.20 (m, 2H), 1.31 (d, J=6.5 Hz, 3H).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08629167B2
출처 데이터셋uspto-grants-2014_01
ORD IDord-97dc625de3fd4b8aa4acb9fa0409a365
출처 메모uspto-grants-2014_01