참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Isopropanol | HCID 3776 | — |
| 반응물 | 3-Amino-1-propanol | HCID 9086 | — |
| 반응물 | Triphenylphosphine | HCID 11776 | — |
| 반응물 | Stannous chloride dihydrate | HCID 61436 | — |
| 반응물 | 1-Methoxy-2-methyl-4-nitrobenzene | HCID 643520 | — |
| 촉매 | Ruthenium trichloride hydrate | HCID 6093376 | — |
| 용매 | 1,4-Dioxane--water (1/1) | HCID 21886435 | — |
| 생성물 | 6-Methoxy-7-methylquinoline | HCID 15534898 | 15.4% |
반응 단계
1-methoxy-2-methyl-4-nitrobenzene (3A) (5 g, 30.0 mmol), 3-amino-1-propanol (0.57 mL, 7.5 mmol), isopropanol (3.43 mL, 4.5 mmol), ruthenium(III) chloride hydrate (156 mg, 0.75 mmol), triphenylphosphine (588 mg, 2.24 mmol), and tin(II) chloride dihydrate (1.69 g, 7.5 mmol) in dioxane/H2O (67 mL/7 mL) were placed in a stainless steel pressure vessel. After the system was flushed with argon, the mixture was stirred at 180° C. for 20 hours. The reaction mixture was filtered through a short silica gel column (ethyl acetate/chloroform mixture) to eliminate inorganic compounds and concentrated under reduced pressure. The organic layer was poured into saturated brine, extracted with chloroform, dried over anhydrous sodium sulfate, and evaporated under reduced pressure. The residual oily material was separated by column chromatography to give the product 3B (200 mg, 15%). LCMS-ESI+ (m/z): 174.2 (M+H)+.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US09296758B2 |
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| 출처 데이터셋 | uspto-grants-2016_03 |
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| ORD ID | ord-777bcf34fd8e427ea76d87be20965b8e |
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| 출처 메모 | uspto-grants-2016_03 |
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