참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Sodium Hydroxide | HCID 14798 | — |
| 반응물 | 3-Cyclopropyl-3-oxopropanenitrile | HCID 9812763 | — |
| 반응물 | (2-Aminophenyl)(4-fluorophenyl)methanone methanesulfonate | HCID 53446970 | — |
| 용매 | Toluene | HCID 1140 | — |
| 생성물 | 2-Cyclopropyl-4-(4'-fluorophenyl)quinoline-3-carbonitrile | HCID 9965738 | 91% |
반응 단계
Into a glass flask having an internal volume of 50 mL, equipped with a stirring apparatus, a thermometer, a reflux condenser and a Dean-Stark apparatus, 10.72 g (6.6 mmol) of 3-cyclopropyl-3-oxopropanenitrile, 1.92 g (6.0 mmol) of 2-amino-4′-fluorobenzophenone methanesulfonate having a purity of 97.3% and 10 mL of toluene were put in an atmosphere of nitrogen, and reaction was carried out under at 110° C. for 2 hours while distilling off the formed water. After completion of the reaction, the reaction liquid was cooled to room temperature, 7.0 mL (7.0 mmol) of a 1 mol/L sodium hydroxide aqueous solution was added thereto to make the reaction liquid basic, followed by liquid separation, and the obtained organic layer was analyzed by high performance liquid chromatography (absolute quantitative analysis), whereupon 1.57 g (yield: 91%) of 2-cyclopropyl-4-(4′-fluorophenyl)quinoline-3-carbonitrile was formed.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US06841681B2 |
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| 출처 데이터셋 | uspto-grants-2005_01 |
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| ORD ID | ord-6d7d89a32988436c84b63e25d2728170 |
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| 출처 메모 | uspto-grants-2005_01 |
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