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HRID 51962作成日:2026年10月26日

Pyridine → 7-(2-Benzyloxy-3-methoxy-benzoylamino)-quinoline-3-carboxylic acid (di-pyridin-2-yl-methyl)-amide

https://huagongshe.com/reaction/51962

反応式

関与物質

役割名称HCID仕込み量
反応物PyridineHCID 1049—
反応物Thionyl ChlorideHCID 24386—
反応物2-(Benzyloxy)-3-methoxybenzoic acidHCID 964395—
反応物7-Amino-quinoline-3-carboxylic acid (di-pyridin-2-yl-methyl)-amideHCID 86585940—
触媒DimethylformamideHCID 6228—
溶媒ChloroformHCID 6212—
生成物7-(2-Benzyloxy-3-methoxy-benzoylamino)-quinoline-3-carboxylic acid (di-pyridin-2-yl-methyl)-amideHCID 8658594234%

反応手順

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).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06713489B2
出典データセットuspto-grants-2004_03
ORD IDord-7c6d04060e1e4a2cb55986e17a5d12d7
出典メモuspto-grants-2004_03