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HRID 351349作成日:2026年10月24日

Triethylamine → 4'-chloro-N-{3-[(diethylamino)methyl]-6-methoxy-7-quinolinyl}[1,1'-biphenyl]-4-carboxamide

https://huagongshe.com/ja/reaction/351349

反応式

関与物質

役割名称HCID仕込み量
反応物TriethylamineHCID 8471—
反応物Oxalyl chlorideHCID 65578—
反応物4-Biphenylcarboxylic acid, 4'-chloro-HCID 616002—
反応物3-[(Diethylamino)methyl]-6-methoxy-7-quinolinylamineHCID 18435942—
触媒DimethylformamideHCID 6228—
溶媒DimethylformamideHCID 6228—
溶媒TetrahydrofuranHCID 8028—
溶媒Ethyl AcetateHCID 8857—
生成物4'-chloro-N-{3-[(diethylamino)methyl]-6-methoxy-7-quinolinyl}[1,1'-biphenyl]-4-carboxamideHCID 1843605813.5%

反応手順

4′-Chloro[1,1′-biphenyl]-4-carboxylic acid (100 mg, 0.430 mmol) was dissolved in tetrahydrofuran (5 ml). To the reaction solution were added oxalyl chloride (0.0375 ml, 0.430 mmol) and one drop of DMF, and the mixture was stirred at room temperature for 1.5 hrs. The reaction solution was concentrated under reduced pressure and the obtained pale-brown crystals were dissolved in DMF (1 ml). Thereto were added a solution of 3-[(diethylamino)methyl]-6-methoxy-7-quinolinylamine (111 mg, 0.430 mmol) obtained in Reference Example 13 in DMF (1 ml) and triethylamine (0.0719 ml, 0.516 mmol), and the mixture was stirred at room temperature for 4 hrs. Ethyl acetate (20 ml) was added to the reaction solution, and the mixture was washed with a mixed solution of aqueous potassium carbonate solution (10 ml) and saturated brine (5 ml), and then with a mixed solution of saturated brine (10 ml) and water (10 ml). The organic layer was purified by NH-silica gel column, and the precipitated crystals were washed with ethyl acetate:isopropyl ether=2:1. The crystals were collected by filtration and dried to give the title compound (27.5 mg) as pale-yellow crystals.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07183415B2
出典データセットuspto-grants-2007_02
ORD IDord-51f39c8bf894482a9608cf77ec3a671b
出典メモuspto-grants-2007_02