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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 334934생성일: 2026년 10월 24일

Diisopropylethylamine → (2,4-Bis-benzyloxy-5-isopropenyl-phenyl)-[4-(3-morpholin-4-yl-propoxy)-1,3-dihydro-isoindol-2-yl]-methanone

https://huagongshe.com/ko/reaction/334934

반응식

참여 물질

역할이름HCID투입량
반응물DiisopropylethylamineHCID 81531—
반응물PyBroPHCID 2733179—
반응물4-(3-Morpholin-4-yl-propoxy)-2,3-dihydro-1H-isoindoleHCID 46915186—
반응물2,4-Bis(benzyloxy)-5-isopropenylbenzoic acidHCID 49864016—
용매DichloromethaneHCID 6344—
용매Ethyl AcetateHCID 8857—
생성물(2,4-Bis-benzyloxy-5-isopropenyl-phenyl)-[4-(3-morpholin-4-yl-propoxy)-1,3-dihydro-isoindol-2-yl]-methanoneHCID 46915345—

반응 단계

A solution of 2,4-bis-benzyloxy-5-isopropenyl-benzoic acid (210 mg, 0.56 mmol) and diisopropylethylamine (0.25 mL, 1.4 mmol) in DCM (5 mL) was treated with bromo-tris-pyrrolidino-phosphonium hexafluorophosphate (PyBrOP) (287 mg, 0.62 mmol). After 1 hour a solution of 4-(3-morpholin-4-yl-propoxy)-2,3-dihydro-1H-isoindole (0.56 mmol, assuming a quantitative yield from the preceding step (C18)) in DCM (5 mL) was added. After 4 hours the mixture was diluted with ethyl acetate and washed with water, 1N sodium hydroxide solution and brine. The organic phase was dried (MgSO4) and concentrated to give a residue which was absorbed onto an SCX column. This was washed with 10% methanol/DCM then the product was eluted with 25% 2M methanolic ammonia/DCM) to afford an impure sample of the intermediate (2,4-bis-benzyloxy-5-isopropenyl-phenyl)-[4-(3-morpholin-4-yl-propoxy)-1,3-dihydro-isoindol-2-yl]-methanone.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08883790B2
출처 데이터셋uspto-grants-2014_11
ORD IDord-81327ceb8aec4685865f7f89e7005ad0
출처 메모uspto-grants-2014_11