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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

반응식

참여 물질

역할이름HCID투입량
반응물Bis(2-chloroethyl) etherHCID 8115—
반응물DiisopropylethylamineHCID 81531—
반응물(5-Amino-1,3-dihydro-isoindol-2-yl)-(2,4-bis-benzyloxy-5-isopropyl-phenyl)-methanoneHCID 66672407—
촉매Tetrabutylammonium IodideHCID 67553—
용매N-methyl-2-pyrrolidoneHCID 13387—
생성물(2,4-Bis-benzyloxy-5-isopropyl-phenyl)-(5-morpholin-4-yl-1,3-dihydro-isoindol-2-yl)-methanoneHCID 59263147—

반응 조건

온도150 °C

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

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07700625B2
출처 데이터셋uspto-grants-2010_04
ORD IDord-ba694863a8344cff8f3d4273b5f878ee
출처 메모uspto-grants-2010_04