참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Dimethylformamide | HCID 6228 | — |
| 반응물 | Acetonitrile | HCID 6342 | — |
| 반응물 | Sodium hydride | HCID 24758 | — |
| 반응물 | 3-(Chloromethyl)-1,2,4-oxadiazole | HCID 2735765 | — |
| 반응물 | 3-(3,4-Dimethyl-benzoyl)-1H-quinolin-4-one | HCID 57754515 | — |
| 생성물 | 3-(3,4-Dimethyl-benzoyl)-1-(5-methyl-isoxazol-3-ylmethyl)-1H-quinolin-4-one | HCID 16730933 | — |
반응 단계
26 mg (0.65 mmol) of sodium hydride (60%) was suspended in 3 mL of anhydrous dimethylformamide and to it was added 138.7 mg (0.50 mmol) of 3-(3,4-dimethyl-benzoyl)-2,3-dihydro-1H-quinolin-4-one 3a and the resultant mixture was stirred at rt for 30 min. Then 77.4 mg (0.65 mmol) of 3-chloromethyl-1,2,4-oxadiazole was added to the reaction solution and the mixture was stirred at 80° C. for 1 h. The reaction solution was quenched by the addition of 10 mL of water. The crude product precipitated out of solution and was isolated by filtration. Purification of the crude product by flash chromatography provided 55 mg of 4cc as a colorless solid: LC-MSD, m/z for C23H20N2O3, [M+H]+=373.4, [M+2H]+=374.4; Reverse phase HPLC (gradient acetonitrile 0.1% TFA 20-95% in 4 min) retention time =2.639 min; 1H NMR (400 MHz, CDCl3/HCl): δ 2.30 (d, 6H), 2.36 (s, 3H), 5.38 (s, 2H), 5.90 (s, 1H), 7.15 (d, 1H), 7.42 (t, 1H), 7.50-7.68 (m, 4H), 8.27 (s, 1H), 8.44 (d, 1H).
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US07557213B2 |
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| 출처 데이터셋 | uspto-grants-2009_07 |
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| ORD ID | ord-b1b7d3dc6c0d410b90c1fceaad4c1d8e |
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| 출처 메모 | uspto-grants-2009_07 |
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