Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1895006생성일: 2026년 10월 26일
3-[hydroxy-(1-triisopropylsilanyl-1H-indol-5-yl)-methyl]-3-phenyl-pyrrolidine-1-carboxylic acid methyl ester → HCID 66688025, 화합물
https://huagongshe.com/reaction/1895006
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | 3-[hydroxy-(1-triisopropylsilanyl-1H-indol-5-yl)-methyl]-3-phenyl-pyrrolidine-1-carboxylic acid methyl ester | HCID 58017239 | — |
| 촉매 | HCID 178418406 | HCID 178418406 | — |
| 용매 | Toluene | HCID 1140 | — |
| 생성물 | HCID 66688025 | HCID 66688025 | 109.5% |
반응 단계
Manganese dioxide (85%, 256 mg, 2.95 mmol) was added to a solution of 3-[hydroxy-(1-triisopropylsilanyl-1H-indol-5-yl)-methyl]-3-phenyl-pyrrolidine-1-carboxylic acid methyl ester (300 mg, 0.59 mmol) in toluene (8 mL). The reaction mixture was heated at 100° C. for 2 hours, then cooled to room temperature and filtered through a celite pad. The filtrate was evaporated under reduced pressure to give 326 mg of 3-phenyl-3-(1-triisopropylsilanyl-1H-indole-5-carbonyl)-pyrrolidine-1-carboxylic acid methyl ester as a colorless foamy oil. A portion of this product (298 mg, 0.59 mmol) was dissolved in THF (8 mL) and a solution of tetrabutylammonium fluoride (1.0 M in THF, 0.60 mL, 0.59 mmol) was added at 0° C. The reaction mixture was stirred at 0° C. for 20 minutes, then was quenched by addition of water. The resulting mixture was extracted with EtOAc, and the combined organic extracts were dried over MgSO4, filtered and evaporated under reduced pressure. The residue was purified by flash chromatography (30% to 50% of EtOAc in hexane) to give 167 mg (81% 2 steps yield) of 3-(1H-indole-5-carbonyl)-3-phenyl-pyrrolidine-1-carboxylic acid methyl ester as a white foam.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US08513425B2 |
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| 출처 데이터셋 | uspto-grants-2013_08 |
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| ORD ID | ord-3746d6a064874b31aef99d4cb3d5d7dc |
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| 출처 메모 | uspto-grants-2013_08 |
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