참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Acetic Acid | HCID 176 | — |
| 반응물 | p-Toluenesulfonic acid | HCID 6101 | — |
| 반응물 | N4-Isobutyl-1,5-naphthyridine-3,4-diamine | HCID 53699038 | — |
| 반응물 | 1,3-dimethoxycarbonyl-O-methylisourea | HCID 85348789 | — |
| 용매 | Methanol | HCID 887 | — |
| 생성물 | HCID 86626310 | HCID 86626310 | — |
반응 단계
A mixture of N4-(2-methylpropyl)[1,5]naphthyridine-3,4-diamine (Gerster et al, U.S. Pat. No. 6,194,425, Example 30 Part A, 4.10 g, 19.0 mmol), 1,3-dimethoxycarbonyl-O-methylisourea (7.21 g, 37.9 mmol), acetic acid (5.69 g, 94.8 mmol), and p-toluenesulfonic acid (3.60 g, 19.0 mmol) in methanol (50 mL) was heated at reflux for 16 hours. The volatiles were removed under reduced pressure, and the residue was dissolved in chloroform (150 mL). The solution was washed sequentially with water (150 mL), aqueous sodium carbonate (150 mL of 4% w/w), water (150 mL), and brine (150 mL) and then concentrated under reduced pressure. The residue was purified by automated flash chromatography (40+M silica cartridge, eluting with 0% to 20% CMA in chloroform) followed by recrystallization from acetonitrile to provide 1.78 g of methyl [1-(2-methylpropyl)-1H-imidazo[4,5-c][1,5]naphthyridin-2-yl]carbamate as a white solid, mp 195-197° C.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US08143270B2 |
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| 출처 데이터셋 | uspto-grants-2012_03 |
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| ORD ID | ord-6678059f397a435994898fa220c42068 |
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| 출처 메모 | uspto-grants-2012_03 |
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