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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 38753생성일: 2026년 10월 24일

Aminoisobutyric acid → 2-((4-Carbamoyl-3-fluorophenyl)amino)-2-methylpropanoic acid

https://huagongshe.com/ko/reaction/38753

반응식

참여 물질

역할이름HCID투입량
반응물Aminoisobutyric acidHCID 6119—
반응물Potassium CarbonateHCID 11430—
반응물2-AcetylcyclohexanoneHCID 13400—
반응물4-Bromo-2-fluorobenzamideHCID 2773331—
촉매Copper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI)HCID 24350—
용매WaterHCID 962—
용매DimethylformamideHCID 6228—
생성물2-((4-Carbamoyl-3-fluorophenyl)amino)-2-methylpropanoic acidHCID 66617902—

반응 조건

온도97.5 °C

반응 단계

4-Bromo-2-fluorobenzamide (0.5 g, 2.29 mmol), 2 aminoisobutyric acid (0.354 g, 3.54 mmol), CuI (87 mg, 0.458 mmol), and K2CO3 (0.790 g, 5.72 mmol) were mixed in DMF (5 mL). H2O (0.5 mL) and TEA (11 mg, 0.1 mmol) were added followed by 2-acetyl cyclohexanone (60 mg, 0.428 mmol).The reaction mixture was heated to 95-100° C. for 48 h. The reaction mixture was diluted with H2O (20 mL) and the aqueous layer was washed with ethyl acetate (20 mL). The aqueous layer was acidified with 1M citric acid to pH 4 and the product was extracted with ethyl acetate (20 mL×3). The combined organic layer was dried over anhydrous Na2SO4 and concentrated under reduced pressure to obtain the product. 1H NMR (DMSO, Freebase): δ (ppm) 7.55-7.45 (t, 1H), 7.20 (bs, 1H), 7.05 (bs, 1H), 6.80 (bs, 1H), 6.35-6.30 (d, 1H), 6.18-6.10 (d, 1H), 1.42 (s, 6H).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08524755B2
출처 데이터셋uspto-grants-2013_09
ORD IDord-793f1188cf4d41e1a8718bd601062328
출처 메모uspto-grants-2013_09