Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
m-Xylyl bromide → 3-(3,4-Dimethyl-benzoyl)-1-(3-methyl-benzyl)-2,3-dihydro-1H-quinolin-4-one
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|---|---|---|
| 반응물 | m-Xylyl bromide | HCID 12099 | — |
| 반응물 | Sodium hydride | HCID 24758 | — |
| 반응물 | 3-(3,4-Dimethyl-benzoyl)-1H-quinolin-4-one | HCID 57754515 | — |
| 용매 | Dimethylformamide | HCID 6228 | — |
| 생성물 | 3-(3,4-Dimethyl-benzoyl)-1-(3-methyl-benzyl)-2,3-dihydro-1H-quinolin-4-one | HCID 67072135 | — |
반응 단계
Compound 4m was prepared following the procedure outlined in Step 3 of Example 1 using 16 mg (0.4 mmol) of sodium hydride (60%), 86 mg (0.31 mmol) of 3-(3,4-dimethyl-benzoyl)-2,3-dihydro-1H-quinolin-4-one 3a, 3 mL of anhydrous dimethylformamide, and 74.0 mg (0.40 mmol) of 3-methylbenzylbromide. The crude product 4m was purified by flash chromatograph to yield 55 mg of colorless solid: LC-MSD, m/z for C26H23NO2, [M+H]+: 382.5, [M+H]+: 383.5; Reverse phase HPLC (gradient acetonitrile 0.1% TFA 20-95% in 4 min) retention time=2.628 min; 1H NMR (400 MHz, CDCl3/HCl): δ 2.3-2.4 (t, 9H), 5.4 (s, 2H), 7.0 (d, 2H), 7.12 (d, 1H), 7.18 (d, 1H), 7.25 (d, 1H), 7.4 (t, 2H), 7.58 (m, 2H), 7.65 (s, 1H), 8.26 (s, 1H), 7.48 (s, 1H).
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 특허 번호 | US07557213B2 |
| 출처 데이터셋 | uspto-grants-2009_07 |
| ORD ID | ord-d1cbefff430f4df5b2e42ab307128bfc |
| 출처 메모 | uspto-grants-2009_07 |