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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

반응식

참여 물질

역할이름HCID투입량
반응물TriethylamineHCID 8471—
반응물1-Ethyl-3-(3'-dimethylaminopropyl)carbodiimideHCID 15908—
반응물1-HydroxybenzotriazoleHCID 75771—
반응물5-(Furan-2-yl)-1,3,4-oxadiazol-2-amineHCID 202185—
반응물6-Cyano-2-phenyl-4-quinolinecarboxylic acidHCID 67204864—
용매DimethylformamideHCID 6228—
생성물6-cyano-N-[5-(2-furyl)-1,3,4-oxadiazol-2-yl]-2-phenyl-4-quinolinecarboxamideHCID 672054421.2%

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

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08466290B2
출처 데이터셋uspto-grants-2013_06
ORD IDord-c97ce47cec8848cebce8b40a524003cc
출처 메모uspto-grants-2013_06