참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Potassium Carbonate | HCID 11430 | — |
| 반응물 | Trimethyl orthoacetate | HCID 15050 | — |
| 반응물 | 3-Phenylpropylamine | HCID 16259 | — |
| 반응물 | 2-(4-Fluoro-3-nitrophenyl)benzoxazole | HCID 21990970 | — |
| 반응물 | HCID 178418361 | HCID 178418361 | — |
| 촉매 | HCID 178418390 | HCID 178418390 | — |
| 용매 | Ethanol | HCID 702 | — |
| 용매 | Methanol | HCID 887 | — |
| 용매 | Water | HCID 962 | — |
| 생성물 | 5-(Benzoxazol-2-yl)-2-methyl-1-(3-phenylpropyl)benzimidazole | HCID 67498064 | 17.8% |
반응 단계
To a suspension of 2-(4-fluoro-3-nitrophenyl)benzoxazole (see Working Example 15-2) (300 mg, 1.16 mmol) in ethanol (5 mL) was added potassium carbonate (176 mg, 1.28 mmol) and 3-phenylpropylamine (189 mg, 1.39 mmol), and this was heated to reflux for 3 hours. After the reaction was complete, this was cooled to room temperature, water was added, and the precipitated crystals were filtered, washed with water and then dried. To a tetrahydrofuran solution (5 mL) of the crystals obtained was added 10% palladium-carbon (50 mg). A hydrogen atmosphere was substituted in the flask, and this was stirred at room temperature for 6 hours. After the reaction was complete, this was filtered through Celite and the filtrate was concentrated. The residue obtained was dissolved in methanol (5 mL), and to this was added 1,1,1-trimethoxyethane (108 mg, 0.896 mmol), and this was heated to reflux for 6 hours. After the reaction was complete, this was concentrated, and the residue obtained was purified by silica gel column chromatography to yield the title compound (58.5 mg, 14% yield) as white crystals.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US08829035B2 |
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| 출처 데이터셋 | uspto-grants-2014_09 |
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| ORD ID | ord-195f30aa87854e2c8186d29248fe96ca |
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| 출처 메모 | uspto-grants-2014_09 |
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