참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | 3-Sulfolene | HCID 6498 | — |
| 반응물 | Potassium Hydroxide | HCID 14797 | — |
| 반응물 | 5-Bromo-1,2,3,4-tetrahydroisoquinoline hydrochloride | HCID 45074003 | — |
| 용매 | Water | HCID 962 | — |
| 용매 | Sodium Bicarbonate | HCID 516892 | — |
| 생성물 | 5-Bromo-2-(1,1-dioxo-tetrahydro-thiophen-3-yl)-1,2,3,4-tetrahydro-isoquinoline | HCID 58317890 | — |
반응 단계
To a solution containing 5-bromo-1,2,3,4-tetrahydroisoquinoline hydrochloride (1.5 g, 6 mmol) and butadiene sulfone (1.2 g, 10.2 mmol) in water (20 mL) is added 1N KOH (10 mL). The reaction mixture is stirred at 70° C. for 24 hours. After cooling to ambient temperature, the reaction mixture is diluted with saturated NaHCO3 solution and extracted with dichloromethane three times. The organic phase is washed with brine and dried over Na2SO4 before drying by rotary evaporation. The crude product is purified by silica gel flash chromatography to afford 5-bromo-2-(1,1-dioxo-tetrahydro-thiophen-3-yl)-1,2,3,4-tetrahydro-isoquinoline as a wax-like solid. MS m/z 330.1 (M+1).
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US08507491B2 |
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| 출처 데이터셋 | uspto-grants-2013_08 |
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| ORD ID | ord-978128e09c794bfa95ffcd1d26089dfe |
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| 출처 메모 | uspto-grants-2013_08 |
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