Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1174011생성일: 2026년 10월 25일
Phthalimide → 2-[2-(4-dipropylaminobutyl)-3-propyl-3H-benzimidazol-5-ylmethyl]isoindole-1,3-dione
https://huagongshe.com/reaction/1174011
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Phthalimide | HCID 6809 | — |
| 반응물 | Triphenylphosphine | HCID 11776 | — |
| 반응물 | [2-(4-dipropylaminobutyl)-3-propyl-3H-benzimidazol-5-yl]methanol | HCID 23079221 | — |
| 반응물 | Diethylazodicarboxylate toluene | HCID 66777355 | — |
| 용매 | Toluene | HCID 1140 | — |
| 생성물 | 2-[2-(4-dipropylaminobutyl)-3-propyl-3H-benzimidazol-5-ylmethyl]isoindole-1,3-dione | HCID 23155501 | 41.9% |
반응 단계
The compound (302 mg) obtained in Example 125-4 was dissolved in toluene (6.0 ml) and added with triphenylphosphine (275 mg) and phthalimide (193 mg), followed by cooling to 0° C. In this solution, a 40% diethyl azodicarboxylate/toluene solution (452 mg) was dropped. After that, the solution was stirred overnight at room temperature. After completion of the reaction, the solvent was distilled off under reduced pressure. The residue was dissolved in chloroform and washed with water. Then, the solution was subjected to extraction with chloroform and the extract was then washed with saturated saline solution. The organic layer was dried with anhydrous sodium sulfate. After filtration, the solvent was distilled off under reduced pressure and the residue was then purified through silica gel column chromatography (chloroform/methanol), thereby obtaining the subject compound (174 mg) as a pale-yellow solid.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US07833991B2 |
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| 출처 데이터셋 | uspto-grants-2010_11 |
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| ORD ID | ord-9cbe0ebce2f34542a9734c2c9d839391 |
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| 출처 메모 | uspto-grants-2010_11 |
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