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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 456412생성일: 2026년 10월 25일

Diisopropylethylamine → 1-(3,4-Dimethoxyphenyl)-4-((S)-hexahydropyrrolo[1,2-a]pyrazin-2-yl)butane-1,4-dione

https://huagongshe.com/reaction/456412

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참여 물질

역할이름HCID투입량
반응물DiisopropylethylamineHCID 81531—
반응물Tetrafluoro-m-phenylenediamine dihydrochlorideHCID 149026—
반응물4-(3,4-Dimethoxyphenyl)-4-oxobutanoic acidHCID 219390—
반응물(6S)-1,4-Diazabicyclo(4.3.0)nonaneHCID 781249—
반응물1,3-Propanediamine, N'-(ethylcarbonimidoyl)-N,N-dimethyl-, monohydrochlorideHCID 2723939—
용매DimethylformamideHCID 6228—
용매DichloromethaneHCID 6344—
용매Ethyl AcetateHCID 8857—
생성물1-(3,4-Dimethoxyphenyl)-4-((S)-hexahydropyrrolo[1,2-a]pyrazin-2-yl)butane-1,4-dioneHCID 24886334—

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온도0 °C

반응 단계

At 0° C., 1-(3-dimethylaminopropyl)-3-ethylcarbodiimide hydrochloride (479 mg, 2.5 mmol) was added to a solution of 3-(3,4-dimethoxybenzoyl)propionic acid (596 mg, 2.5 mmol) and 3-hydroxy-3H-dihydrobenzo[d][1,2,3]triazin-4-one (408 mg, 2.5 mmol) in a mixture of dichloromethane (10 ml) and N,N-dimethylformamide (10 ml). The reaction mixture was stirred for 25 min at 0° C. A solution of the crude dihydrochloride salt of (S)-octahydro-pyrrolo[1,2-a]pyrazine in N,N-dimethylformamide (4 ml) and ethyldiisopropylamine (3.0 ml, 17.5 mmol) were added successively. The reaction mixture was stirred for 16 hours, while it was warming up to room temperature. It was diluted with ethyl acetate (200 ml) and washed with a saturated aqueous solution of sodium hydrogen carbonate. The aqueous phase was extracted with ethyl acetate (2×100 ml). The combined organic layers were dried over magnesium sulphate. The solvent was removed in vacuo. The crude product was purified by HPLC on a C18-reversed phase column, using a mixture of 1% trifluoroacetic acid in water and acetonitrile as eluent, to give 148 mg of the title compound.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07186721B2
출처 데이터셋uspto-grants-2007_03
ORD IDord-b1dd81d26a0a444c98d18ffcf9702fb7
출처 메모uspto-grants-2007_03