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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 51962생성일: 2026년 10월 25일

Pyridine → HCID 86585942, 화합물

https://huagongshe.com/reaction/51962

반응식

참여 물질

역할이름HCID투입량
반응물PyridineHCID 1049—
반응물Thionyl ChlorideHCID 24386—
반응물2-(Benzyloxy)-3-methoxybenzoic acidHCID 964395—
반응물7-Amino-quinoline-3-carboxylic acid (di-pyridin-2-yl-methyl)-amideHCID 86585940—
촉매DimethylformamideHCID 6228—
용매ChloroformHCID 6212—
생성물HCID 86585942HCID 8658594234%

반응 단계

A mixture of 2-benzyloxy-3-methoxybenzoic acid (109 mg, 0.42 mmol), thionyl chloride (5 ml) and 1 drop dimethylformamide was heated under reflux for 2 hr. The thionyl chloride was removed in vacuo, with traces being removed by adding methylene chloride and concentrating the solution in vacuo. The resulting 2-benzyloxy-3-methoxybenzoyl chloride was dissolved in chloroform and the solution was added dropwise to a solution of 7-amino-quinoline-3-carboxylic acid (di-pyridin-2-yl-methyl)-amide (75 mg, 0.21 mmol), 4-(N,N-dimethylaminopyridine) (DIMAP) (3 mg, 0.02 mmol) and pyridine (0.068 ml, 0.84 mmol) in chloroform at room temperature. The resulting solution was heated under reflux for 3 hr, then cooled to room temperature and concentrated to dryness in vacuo. The residue was dissolved in ethyl acetate, washed sequentially with water and brine, dried over anhydrous sodium sulfate and concentrated to dryness in vacuo. The residue (960 mg) was purified by column chromatography on silica gel, eluting with 98:2 chloroform/methanol to yield the title compound as a solid (40.3 mg, 34% yield).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06713489B2
출처 데이터셋uspto-grants-2004_03
ORD IDord-7c6d04060e1e4a2cb55986e17a5d12d7
출처 메모uspto-grants-2004_03