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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

반응식

참여 물질

역할이름HCID투입량
반응물TriethylamineHCID 8471—
반응물Tri-o-tolylphosphineHCID 80271—
반응물7-Amino-2,3-dihydro-1H-isoindol-1-oneHCID 16228923—
반응물4-Methyl-7-[1-(tert-butoxycarbonyl)-5-(piperidinomethyl)indol-2-yl]isoindolinoneHCID 68489003—
반응물7-Iodo-4-methylisoindolinoneHCID 68489093—
촉매palladium(II) acetateHCID 167845—
용매AcetonitrileHCID 6342—
생성물7-[1-(Tert-butoxycarbonyl)-5-(piperidinomethyl)indol-2-yl]isoindolinoneHCID 6849081356%

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

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07745641B2
출처 데이터셋uspto-grants-2010_06
ORD IDord-fd568bdb36544647841062cdafaa8ae0
출처 메모uspto-grants-2010_06