Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
m-Xylyl bromide → 3-(3-Methyl-benzoyl)-1-(3-methyl-benzyl)-1H-quinolin-4-one
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|---|---|---|
| 반응물 | m-Xylyl bromide | HCID 12099 | — |
| 반응물 | Sodium hydride | HCID 24758 | — |
| 반응물 | 3-(3-methyl-benzoyl)-2,3-dihydro-1H-quinolin-4-one | HCID 67071952 | — |
| 용매 | Dimethylformamide | HCID 6228 | — |
| 생성물 | 3-(3-Methyl-benzoyl)-1-(3-methyl-benzyl)-1H-quinolin-4-one | HCID 16730853 | 50.1% |
반응 단계
Compound 4y was prepared following the procedure outlined in Step 3 of Example 1 using 26 mg (0.65 mmol) of sodium hydride (60%), 132 mg (0.50 mmol) of 3-(3-methyl-benzoyl)-2,3-dihydro-1H-quinolin-4-one, 3 mL of anhydrous dimethylformamide, and 120 mg (0.65 mmol) of 3-methylbenzylbromide. The crude product was purified by flash chromatography to yield 92 mg of a colorless solid 4y: LC-MSD, m/z for C25H21NO2, [M+H]+=368.5, [M+2H]+=369.5; Reverse phase HPLC (gradient acetonitrile 0.1% TFA 20-95% in 4 min) retention time=2.586 min; 1H NMR (400 MHz, CDCl3/HCl): δ 2.37 (s, 3H), 2.42 (s, 3H), 5.39 (s, 2H), 7.01 (d, 2H), 7.15 (d, 1H), 7.22-7.44 (m, 5H), 7.55-7.58 (m, 3H), 8.29 (s, 1H), 8.47 (d, 1H).
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 특허 번호 | US07557213B2 |
| 출처 데이터셋 | uspto-grants-2009_07 |
| ORD ID | ord-90fef07af96448c2948cb4a7c9a94fe4 |
| 출처 메모 | uspto-grants-2009_07 |