Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 411598생성일: 2026년 10월 26일
Sodium Bicarbonate → 6-Fluoro-3-[1-(8-methoxy-2,3-dihydro-1,4-benzodioxin-2-ylmethyl)-1,2,3,6-tetrahydro-pyridin-4-yl]-1H-indole
https://huagongshe.com/reaction/411598
참여 물질
| 역할 | 이름 | HCID | 투입량 |
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| 반응물 | Sodium Bicarbonate | HCID 516892 | — |
| 반응물 | 6-fluoro-3-(1,2,3,6-tetrahydropyridin-4-yl)-1H-indole | HCID 11053072 | — |
| 반응물 | [(2R)-8-Methoxy-2,3-dihydro-benzo[1,4]dioxin-2-yl]methyl 4-methylbenzenesulfonate | HCID 11792133 | — |
| 용매 | tetrahydrofuran N,N-dimethylformamide | HCID 21974620 | — |
| 생성물 | 6-Fluoro-3-[1-(8-methoxy-2,3-dihydro-1,4-benzodioxin-2-ylmethyl)-1,2,3,6-tetrahydro-pyridin-4-yl]-1H-indole | HCID 10271950 | — |
반응 단계
[(2R)-8-Methoxy-2,3-dihydro-benzo[1,4]dioxin-2-yl]methyl 4-methylbenzenesulfonate (0.30 g, 0.86 mmole), 6-fluoro-3-(1,2,3,6-tetrahydro-4-pyridinyl)-1H-indole (0.60 g, 2.7 mmole) and sodium bicarbonate (0.80 g) were added to a mixture of dimethylformamide/tetrahydrofuran (1:1 v/v, 20 mL) and the reaction mixture was refluxed under nitrogen for 18 hours. The solvent was evaporated and the residue partitioned between 400 mL each of water and methylene chloride. The layers were separated and the methylene chloride solution was washed with water and saturated aqueous sodium chloride solution, dried over anhydrous potassium carbonate and filtered. The filtrate was evaporated in vacuum and the residue crystallized from chloroform containing 3% methanol, giving 0.23 g (68%) of the (S)-enantiomer of the title compound as an off-white solid, m.p. 184-185° C.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US06559169B2 |
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| 출처 데이터셋 | uspto-grants-2003_05 |
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| ORD ID | ord-acc11fd42515437f9500a243b1ae8555 |
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| 출처 메모 | uspto-grants-2003_05 |
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