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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 896055생성일: 2026년 10월 25일

Diisopropylethylamine → 8-(6-Ethynyl-isoquinolin-4-ylmethyl)-3-isobutyl-1-methyl-3,7-dihydro-purine-2,6-dione

https://huagongshe.com/reaction/896055

반응식

참여 물질

역할이름HCID투입량
반응물DiisopropylethylamineHCID 81531—
반응물4,5-Diamino-3-isobutyl-1-methylpyrimidine-2,6-dioneHCID 4110339—
반응물(6-Ethynyl-isoquinolin-4-yl)-acetic acidHCID 22226561—
용매DimethylformamideHCID 6228—
생성물8-(6-Ethynyl-isoquinolin-4-ylmethyl)-3-isobutyl-1-methyl-3,7-dihydro-purine-2,6-dioneHCID 22226484—

반응 단계

(6-Ethynyl-isoquinolin-4-yl)-acetic acid (58 mg, 0.28 mmol) is dissolved in DMF (1 ml) and O-(7-azabenzotriazo-1-yl)-N,N,N′,N′-tetramethyluronium hexafluorophosphate (0.125 g, 0.33 mmol) and Hunig's base (0.180 ml, 1.03 mmol) are added, followed by a solution of 5,6-diamino-1-isobutyl-3-methyl-1H-pyrimidine-2,4-dione (58 mg, 0.28 mmol) in DMF (0.7 ml). The reaction is stirred at room temperature for 2 hours. The solvent is evaporated and the residue purified by flash column chromatography (30:1 dichloromethane-methanol elution). The intermediate is dissolved in methanol (2 ml) and water (2.75 ml) added, followed by 4M aqueous sodium hydroxide (0.25 ml). The reaction is heated at 40° C. for 2 hours, then stirred for 16 hours at ambient temperature. The solvent is evaporated and the crude product purified by flash column chromatography (30:1 dichloromethane-methanol elution) to afford 8-(6-ethynyl-isoquinolin4-ylmethyl)-3-isobutyl-1-methyl-3,7-dihydro-purine-2,6-dione, [MH]+ 388.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06919337B2
출처 데이터셋uspto-grants-2005_07
ORD IDord-af79822438bc435b9708b830e40632f2
출처 메모uspto-grants-2005_07