Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1259853생성일: 2026년 10월 26일
Triethylamine → 6-cyano-N-[5-(2-furyl)-1,3,4-oxadiazol-2-yl]-2-phenyl-4-quinolinecarboxamide
https://huagongshe.com/reaction/1259853
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Triethylamine | HCID 8471 | — |
| 반응물 | 1-Ethyl-3-(3'-dimethylaminopropyl)carbodiimide | HCID 15908 | — |
| 반응물 | 1-Hydroxybenzotriazole | HCID 75771 | — |
| 반응물 | 5-(Furan-2-yl)-1,3,4-oxadiazol-2-amine | HCID 202185 | — |
| 반응물 | 6-Cyano-2-phenyl-4-quinolinecarboxylic acid | HCID 67204864 | — |
| 용매 | Dimethylformamide | HCID 6228 | — |
| 생성물 | 6-cyano-N-[5-(2-furyl)-1,3,4-oxadiazol-2-yl]-2-phenyl-4-quinolinecarboxamide | HCID 67205442 | 1.2% |
반응 단계
HOBt (0.0351 g, 0.260 mmol) and 1-ethyl-3-(3-dimethylaminopropyl)carbodiimide (EDC) (0.0460 g, 0.240 mmol) were added to a dimethylformamide (5.0 mL) solution of 6-cyano-2-phenyl-4-quinolinecarboxylic acid (0.0548 g, 0.200 mmol) described in Reference Example 22 and triethylamine (0.0223 g, 0.220 mmol), and the mixture was stirred at room temperature for 30 minutes. Commercially available 2-amino-5-(2-furyl)-1,3,4-oxadiazole (0.0332 g, 0.220 mmol) was added thereto, and the mixture was stirred at room temperature. The reaction solution was subjected to extraction with dichloromethane, washed with water and saturated saline, and dried over anhydrous sodium sulfate, and then, the solvent was distilled off. The obtained residue was fractionated by silica gel column chromatography, and the solvent was distilled off to obtain the title compound (0.001 g, 0.0024 mmol) as an amorphous substance.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US08466290B2 |
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| 출처 데이터셋 | uspto-grants-2013_06 |
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| ORD ID | ord-c97ce47cec8848cebce8b40a524003cc |
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| 출처 메모 | uspto-grants-2013_06 |
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