참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Boron tribromide | HCID 25134 | — |
| 반응물 | HCID 178448740 | HCID 178448740 | — |
| 용매 | Dichloromethane | HCID 6344 | — |
| 생성물 | HCID 178448739 | HCID 178448739 | 78% |
반응 단계
2-Butyl-5-hydroxy-6-isopropyl-4-(7-methoxy-1, 1-dioxo-1,2-dihydro-1λ6-benzo[1,2,4]thiadiazin-3-yl)-2H-pyridazin-3-one (5e) (56 mg) was dissolved in 3 mL of methylene chloride. BBr3 (466 μL, 1.0 M in methylene chloride) was added and the mixture was stirred at room temperature for 1.5 hours. LC-MS result showed the incompletion of the reaction. BBr3 (0.5 mL, 1.0 M) was added and the reaction mixture was continued to shake at room temperature overnight. LC-MS confirmed that the reaction was close to completion. The reaction mixture was poured onto ice (10 mL), extracted with CHCl3 (20 mL×3). The organic layer was dried over MgSO4, filtered, concentrated under reduced pressure and further purified by flash chromatography on silica gel to give the desired product (5f) (42.2 mg) in 78.0% yield. 1H NMR (400 MHz, CDCl3): δ 7.46 (d, 1H, J=2.8 Hz), 7.16-7.26 (m, 2 H), 4.20 (t, 2H, J=7.2 Hz), 3.34 (m, J=6.8 Hz, 1H), 1.81 (m, 2H), 1.41 (m, 2H), 1.29 (d, 6H, J=6.8 Hz), 1.00 (t, 3H, J=7.4 Hz); LC-MS (ESI+): m/e=407.1 [M+1]+ (exact MS: 406.13).
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US07425552B2 |
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| 출처 데이터셋 | uspto-grants-2008_09 |
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| ORD ID | ord-f17c5e88cce94e94a4c4b6a4f94a6f69 |
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| 출처 메모 | uspto-grants-2008_09 |
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