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HRID 1259847생성일: 2026년 10월 27일

Dichloromethane → N-[5-(2-furyl)-1,3,4-oxadiazol-2-yl]-8-methyl-2-(2-thienyl)-4-quinolinecarboxamide

https://huagongshe.com/reaction/1259847

반응식

참여 물질

역할이름HCID투입량
반응물DichloromethaneHCID 6344—
반응물5-(Furan-2-yl)-1,3,4-oxadiazol-2-amineHCID 202185—
반응물8-Methyl-2-(thiophen-2-yl)quinoline-4-carboxylic acidHCID 3604519—
반응물Triphenylphosphine bromideHCID 22470945—
용매PyridineHCID 1049—
생성물N-[5-(2-furyl)-1,3,4-oxadiazol-2-yl]-8-methyl-2-(2-thienyl)-4-quinolinecarboxamideHCID 6720422612.5%

반응 단계

Triphenylphosphine bromide (352 mg, 0.80 mmol) was added to a methylene chloride (1 mL) solution of commercially available 8-methyl-2-(2-thienyl)-4-quinolinecarboxylic acid (108 mg, 0.40 mmol), and the mixture was stirred at room temperature for 1 hour. The reaction solution was added to a pyridine (3 mL) solution of 2-amino-5-(2-furyl)-1,3,4-oxadiazole (90.7 mg, 0.60 mmol), and the mixture was stirred at room temperature for 2 hours and then heated with stirring overnight at 60° C. The reaction solution was concentrated. After that, to the residue, water was added, and the deposited solid was collected by filtration, washed with water, dried, and then purified by preparative HPLC to obtain the title compound (22 mg, 0.05 mmol).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08466290B2
출처 데이터셋uspto-grants-2013_06
ORD IDord-baaa908b98d24ca3bb60f5f72697d863
출처 메모uspto-grants-2013_06