참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Aminoisobutyric acid | HCID 6119 | — |
| 반응물 | Potassium Carbonate | HCID 11430 | — |
| 반응물 | 2-Acetylcyclohexanone | HCID 13400 | — |
| 반응물 | 4-Bromo-2-fluorobenzamide | HCID 2773331 | — |
| 촉매 | Copper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI) | HCID 24350 | — |
| 용매 | Water | HCID 962 | — |
| 용매 | Dimethylformamide | HCID 6228 | — |
| 생성물 | 2-((4-Carbamoyl-3-fluorophenyl)amino)-2-methylpropanoic acid | HCID 66617902 | — |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US08524755B2 |
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| 출처 데이터셋 | uspto-grants-2013_09 |
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| ORD ID | ord-793f1188cf4d41e1a8718bd601062328 |
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| 출처 메모 | uspto-grants-2013_09 |
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