Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1840935생성일: 2026년 10월 26일
Hydrochloric Acid → 2-(2-{4-[1-(4-fluoro-benzyl)-1H-indol-3-yl]-piperidin-1-yl}-ethoxy)-benzoic acid
https://huagongshe.com/reaction/1840935
참여 물질
| 역할 | 이름 | HCID | 투입량 |
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| 반응물 | Hydrochloric Acid | HCID 313 | — |
| 반응물 | Sodium hydride | HCID 24758 | — |
| 반응물 | 4-Fluorobenzyl bromide | HCID 68021 | — |
| 반응물 | methyl 2-{2-[4-(1H-indol-3-yl)-piperidin-1-yl]-ethoxy}-benzoate | HCID 11440344 | — |
| 용매 | Dimethylformamide | HCID 6228 | — |
| 생성물 | 2-(2-{4-[1-(4-fluoro-benzyl)-1H-indol-3-yl]-piperidin-1-yl}-ethoxy)-benzoic acid | HCID 9847633 | 84% |
반응 단계
0.02 g (0.42 mmol) of a dispersion of 60% NaH in mineral oil were added to a solution of 0.06 g (0.15 mmol) of 2-{2-[4-(1H-indol-3-yl)-piperidin-1-yl]-ethoxy}-benzoic acid methyl ester prepared in step D in 1 mL of anhydrous DMF under nitrogen atmosphere. After stirring 30 minutes at room temperature 0.026 mL (0.21 mmol) of 4-fluoro-benzyl bromide were added and the mixture was stirred for 18 hours. After addition of 0.09 g (0.12 mmol) of 3-(3-mercapto-phenyl)-propanamido-methyl-polystyrene in 1 mL of DMF the mixture was stirred overnight at room temperature. 0.1 mL of 2N HCl were added to the reaction mixture and the crude-was filtered. The solvent was removed under reduced pressure and the crude mixture was purified using a 500 mg Varian C18 chromatography column affording 0.059 g (84% yield) of 2-(2-{4-[1-(4-fluoro-benzyl)-1H-indol-3-yl]-piperidin-1-yl}-ethoxy)-benzoic acid.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US06683096B2 |
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| 출처 데이터셋 | uspto-grants-2004_01 |
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| ORD ID | ord-74e3a4d7fc9f401dbb9670558390d002 |
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| 출처 메모 | uspto-grants-2004_01 |
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