Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 21191생성일: 2026년 10월 25일
Triethylamine → 7-[1-(Tert-butoxycarbonyl)-5-(piperidinomethyl)indol-2-yl]isoindolinone
https://huagongshe.com/reaction/21191
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Triethylamine | HCID 8471 | — |
| 반응물 | Tri-o-tolylphosphine | HCID 80271 | — |
| 반응물 | 7-Amino-2,3-dihydro-1H-isoindol-1-one | HCID 16228923 | — |
| 반응물 | 4-Methyl-7-[1-(tert-butoxycarbonyl)-5-(piperidinomethyl)indol-2-yl]isoindolinone | HCID 68489003 | — |
| 반응물 | 7-Iodo-4-methylisoindolinone | HCID 68489093 | — |
| 촉매 | palladium(II) acetate | HCID 167845 | — |
| 용매 | Acetonitrile | HCID 6342 | — |
| 생성물 | 7-[1-(Tert-butoxycarbonyl)-5-(piperidinomethyl)indol-2-yl]isoindolinone | HCID 68490813 | 56% |
반응 단계
In a similar manner to Step 2 of Example 1, a mixture of 7-iodo-4-methylisoindolinone and 7-iodoisoindolinone (10/1, 40.5 mg, 0.149 mmol) was dissolved in acetonitrile (3.24 mL), and the solution was treated with Compound BD (107 mg, 0.298 mmol), palladium acetate (2.7 mg, 0.012 mmol), tri(o-tolyl)phosphine (7.3 mg, 0.024 mmol) and triethylamine (0.208 mL, 1.49 mmol), followed by purification by preparative thin-layer chromatography (chloroform/methanol=12/1) to obtain a mixture of 4-methyl-7-[1-(tert-butoxycarbonyl)-5-(piperidinomethyl)indol-2-yl]isoindolinone and 7-[1-(tert-butoxycarbonyl)-5-(piperidinomethyl)indol-2-yl]isoindolinone (38.2 mg, ratio 92.9/7.1, yield 56%). 4-methyl-7-[1-(tert-butoxycarbonyl)-5-(piperidinomethyl)indol-2-yl]isoindolinone
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US07745641B2 |
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| 출처 데이터셋 | uspto-grants-2010_06 |
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| ORD ID | ord-fd568bdb36544647841062cdafaa8ae0 |
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| 출처 메모 | uspto-grants-2010_06 |
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