Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 644639생성일: 2026년 10월 24일
Bis(2-chloroethyl) ether → (2,4-Bis-benzyloxy-5-isopropyl-phenyl)-(5-morpholin-4-yl-1,3-dihydro-isoindol-2-yl)-methanone
https://huagongshe.com/ko/reaction/644639
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Bis(2-chloroethyl) ether | HCID 8115 | — |
| 반응물 | Diisopropylethylamine | HCID 81531 | — |
| 반응물 | (5-Amino-1,3-dihydro-isoindol-2-yl)-(2,4-bis-benzyloxy-5-isopropyl-phenyl)-methanone | HCID 66672407 | — |
| 촉매 | Tetrabutylammonium Iodide | HCID 67553 | — |
| 용매 | N-methyl-2-pyrrolidone | HCID 13387 | — |
| 생성물 | (2,4-Bis-benzyloxy-5-isopropyl-phenyl)-(5-morpholin-4-yl-1,3-dihydro-isoindol-2-yl)-methanone | HCID 59263147 | — |
반응 단계
A mixture of (5-amino-1,3-dihydro-isoindol-2-yl)-(2,4-bis-benzyloxy-5-isopropyl-phenyl)-methanone (100 mg; 0.2 mmol), bis(2-chloroethyl)ether (30 μl; 1;1 equiv.), Hunigs base (125 μl; 3.5 equiv.) and tetrabutylammonium iodide (10 mg) in NMP (1 ml) was heated in a CEM microwave synthesiser at 150° C. for 30 minutes. A further 30 μl of Hunigs base and 125 μl of bis(2-chloroethyl)ether were added and heating repeated for the same time. The reaction mixture was partitioned between EtOAc and saturated NH4Cl solution, the EtOAc layer was separated, washed with more saturated NH4Cl solution, then brine, dried (MgSO4) and evaporated. Purification by flash column chromatography (1:2 then 1:1 then 2:1 EtOAc/P.E. as eluant) gave 60 mg of (2,4-bis-benzyloxy-5-isopropyl-phenyl)-(5-morpholin-4-yl-1,3-dihydro-isoindol-2-yl)-methanone. MS: [M+H]+ 563.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US07700625B2 |
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| 출처 데이터셋 | uspto-grants-2010_04 |
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| ORD ID | ord-ba694863a8344cff8f3d4273b5f878ee |
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| 출처 메모 | uspto-grants-2010_04 |
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