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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 21004생성일: 2026년 10월 23일

Triethylamine → Phthalimide

https://huagongshe.com/ko/reaction/21004

반응식

참여 물질

역할이름HCID투입량
반응물TriethylamineHCID 8471—
반응물(E)-3-amino-4-(2-methoxycarbonylvinyl)-6-bromophthalimideHCID 68491786—
촉매Tri-o-tolylphosphineHCID 80271—
촉매palladium(II) acetateHCID 167845—
용매AcetonitrileHCID 6342—
생성물PhthalimideHCID 6809225.1%

반응 단계

In a similar manner to Step 2 of Example 1, (E)-3-amino-4-(2-methoxycarbonylvinyl)-6-bromophthalimide (100 mg, 0.308 mmol) was dissolved in acetonitrile (7 mL), and the solution was treated with Compound BB (292 mg, 0.616 mmol), palladium acetate (5.5 mg, 0.025 mmol), tri(o-tolyl)phosphine (15 mg, 0.049 mmol) and triethylamine (0.429 mL, 3.08 mmol), followed by purification by preparative thin-layer chromatography (chloroform/acetonitrile=6/1) to obtain (E)-3-amino-4-(2-methoxycarbonylvinyl)-6-(tert-butoxycarbonyl)-5-[4-(tert-butoxycarbonyl)piperazin-1-ylcarbonyl]indol-2-yl)phthalimide (102 mg, yield 49%).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07745641B2
출처 데이터셋uspto-grants-2010_06
ORD IDord-bacf4084fd1e45ed9900c8c00955c92f
출처 메모uspto-grants-2010_06