Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1714747생성일: 2026년 10월 25일
8-Iodo-3-(phenylsulfonyl)quinoline → (1S,4S)-5-(3-benzenesulfonyl-quinolin-8-yl)-2,5-diaza-bicyclo[2.2.1]heptane-2-carboxylic acid tert-butyl ester
https://huagongshe.com/reaction/1714747
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | 8-Iodo-3-(phenylsulfonyl)quinoline | HCID 11406774 | — |
| 반응물 | (1S,4S)-2-Boc-2,5-diazabicyclo[2.2.1]heptane | HCID 11521263 | — |
| 반응물 | Sodium t-butoxide | HCID 23676156 | — |
| 촉매 | Di-palladium tetrakis-(dibenzylidene acetone) | HCID 11615059 | — |
| 촉매 | Bis(cyclopenta-2,4-dien-1-yl(phenyl)phosphane);iron(2+) | HCID 133083342 | — |
| 생성물 | (1S,4S)-5-(3-benzenesulfonyl-quinolin-8-yl)-2,5-diaza-bicyclo[2.2.1]heptane-2-carboxylic acid tert-butyl ester | HCID 67313656 | 70% |
반응 단계
3-sulfonyl-8-iodo quinoline (D6) (200 mg, 0.48 mMol), (1S,4S)-2,5-diaza-bicyclo[2.2.1]heptane-2-carboxylic acid tert-butyl ester (95 mg, 0.48 mmol), sodium tbutoxide (65 mg, 0.68 mmol), di-palladium tetrakis-(dibenzylidene acetone) (88 mg, 0.1 mmol) and 1,1′-diphenylphosphino ferrocene (161 mg, 0.3 mMol) were suspended in degassed dry dioxan (2 ml). The mixture was stirred under argon at 40° C. for 16 hours. The solvent was removed and the residue was purified by chromatography on silica using 30% ethyl acetate in hexane to afford (1S,4S)-5-(3-benzenesulfonyl-quinolin-8-yl)-2,5-diaza-bicyclo[2.2.1]heptane-2- carboxylic acid tert-butyl ester in 70% yield. This material (160 mg) was treated with 4M hydrochloric acid (1 ml) and dioxan (1 ml) with stirring at 80° C. for 30 mins. The solvent was removed to afford the title compound E43 as a yellow solid;
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US07799774B2 |
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| 출처 데이터셋 | uspto-grants-2010_09 |
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| ORD ID | ord-a9b24f3efb2049dc8a61a6da38d768a5 |
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| 출처 메모 | uspto-grants-2010_09 |
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