참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Sodium Hydroxide | HCID 14798 | — |
| 반응물 | 2,4-Heptanedione, 6-methyl- | HCID 76354 | — |
| 반응물 | HCID 178418668 | HCID 178418668 | — |
| 용매 | Water | HCID 962 | — |
| 생성물 | 4-Isobutyl-2-(3-isobutyl-5-methylpyrazol-1-yl)-6-methylpyrimidine | HCID 53307246 | 4% |
| 생성물 | 4-Isobutyl-2-(5-isobutyl-3-methylpyrazol-1-yl)-6-methylpyrimidine | HCID 53307247 | 50% |
반응 단계
To aminoguanidine hydrochloride (1.59 g, 14.4 mmol), water (5 ml), sodium hydroxide (576 mg, 14.4 mmol), and 6-methyl-2,4-heptanedione (manufactured by Tokyo Chemical Industry, purity: 97.0% or higher) (4.50 g, 31.6 mmol) were added, and then stirred at 80° C. for 8 hours. To the reaction mixture, water (30 ml) was added, and the extraction was carried out with ethyl acetate (10 ml). The extract was washed with saturated brine, dried with anhydrous sodium sulfate, and then concentrated. The obtained residue (3.83 g) was subjected to silica gel column chromatography (80 g of silica gel, chloroform to chloroform:methanol=100:1) to obtain 4-isobutyl-2-(3-isobutyl-5-methylpyrazol-1-yl)-6-methylpyrimidine (181 mg, 4%) and 4-isobutyl-2-(5-isobutyl-3-methylpyrazol-1-yl)-6-methylpyrimidine (2.05 g, 50%).
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US08592582B2 |
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| 출처 데이터셋 | uspto-grants-2013_11 |
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| ORD ID | ord-2169f77453814d4d9f836f3b947affd6 |
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| 출처 메모 | uspto-grants-2013_11 |
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