참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Water | HCID 962 | — |
| 반응물 | Iodoethane | HCID 6340 | — |
| 반응물 | Potassium Hydroxide | HCID 14797 | — |
| 반응물 | 7-Bromo-4,4,6-trimethyl-3,4-dihydro-1H-quinoline-2-one | HCID 21966423 | — |
| 용매 | Dimethyl Sulfoxide | HCID 679 | — |
| 생성물 | 7-bromo-1,4,4,6-tetramethyl-3,4-dihydro-1H-quinoline-2-one | HCID 21966429 | 104.5% |
반응 단계
A mixture of powdered potassium hydroxide (3.35 g, 59.67 mmol) in DMSO (40 mL) was stirred at 0° C. for 10 min. 7-bromo-4,4,6-trimethyl-3,4- dihydro-1H-quinoline-2-one (Example 1e) (8.0 g, 29.83 mmol) was added cautiously, followed immediately by the addition of ethyl iodide (12 mL, 149.17 mmol). The reaction mixture was kept at 0° C. for 30 min then slowly warmed up to room temperature and stirred overnight at room temperature. The reaction mixture was poured into water and extracted with dichloromethane washed with water and brine, dried (MgSO4), filtered and evaporated to give 8.8 g of 7-bromo-1,4,4,6-tetramethyl-3,4-dihydro-1H-quinoline-2-one and used without further purification in the Suzuki coupling (step a): 1H NMR (300 MHz; CDCl3): 1.24 (t, J=7.2 Hz, 1 H), 1.25 (s, 6 H), 2.37 (s, 3 H), 2.45 (s, 2 H), 3.98 (q, 2 H), 7.13 (s, 1 H), 7.18 (s, 1 H).
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US07102000B2 |
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| 출처 데이터셋 | uspto-grants-2006_09 |
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| ORD ID | ord-65611467eb1f4fa994c040d3141ab846 |
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| 출처 메모 | uspto-grants-2006_09 |
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