Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 896056생성일: 2026년 10월 25일
Diisopropylethylamine → 3-Isobutyl-8-(6-methoxy-isoquinolin-4-ylmethyl)-1-methyl-3,7-dihydro-purine-2,6-dione
https://huagongshe.com/reaction/896056
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Diisopropylethylamine | HCID 81531 | — |
| 반응물 | 4,5-Diamino-3-isobutyl-1-methylpyrimidine-2,6-dione | HCID 4110339 | — |
| 반응물 | (6-Methoxy-isoquinolin-4-yl)-acetic acid | HCID 22226532 | — |
| 용매 | Acetonitrile | HCID 6342 | — |
| 생성물 | 3-Isobutyl-8-(6-methoxy-isoquinolin-4-ylmethyl)-1-methyl-3,7-dihydro-purine-2,6-dione | HCID 9821924 | — |
반응 단계
A suspension of (6-methoxy-isoquinolin4-yl)-acetic acid (3.5 g, 13.82 mmol) in acetonitrile (70 ml) is treated sequentially with Hunig's base (6.15 ml, 36 mmol), O-(7-benzotriazo-1-yl)-N,N,N′,N′-tetramethyluronium hexafluorophosphate (6.29 g, 16.6 mmol) and 5,6-diamino-1-isobutyl-3-methyl-1H-pyrimidine-2,4-dione (3.22 g, 15.2 at mmol) while the solution is stirred at room temperature. The reaction is stirred at ambient temperature for 2 h, prior to evaporation of the solvent. The residue is tritruated with ethyl acetate (50 ml) filtered and washed with ethyl acetate and then dried at 50° C. under reduced pressure. The resulting intermediate is suspended in a mixture of methanol (30 ml) and 4M aqueous sodium hydroxide (60 ml) and heated at 80° C. for 45 minutes. This suspension is neutralized with acetic acid and cooled to 0-5° C. overnight. The resultant solid is collected by filtration, and washed with methanol/water 1:9 (30 ml) followed by methanol (30 ml). Drying under high vacuum at 50° C. affords 3-isobutyl-8-(6-methoxy-isoquinolin-4-ylmethyl)-1-methyl-3,7-dihydro-purine-2,6-dione, [MH]+ 394.5.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US06919337B2 |
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| 출처 데이터셋 | uspto-grants-2005_07 |
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| ORD ID | ord-6774e6ac959c4ec79778227db821f929 |
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| 출처 메모 | uspto-grants-2005_07 |
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