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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 351349생성일: 2026년 10월 24일

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

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

반응식

참여 물질

역할이름HCID투입량
반응물TriethylamineHCID 8471—
반응물Oxalyl chlorideHCID 65578—
반응물4-Biphenylcarboxylic acid, 4'-chloro-HCID 616002—
반응물3-[(Diethylamino)methyl]-6-methoxy-7-quinolinylamineHCID 18435942—
촉매DimethylformamideHCID 6228—
용매DimethylformamideHCID 6228—
용매TetrahydrofuranHCID 8028—
용매Ethyl AcetateHCID 8857—
생성물4'-chloro-N-{3-[(diethylamino)methyl]-6-methoxy-7-quinolinyl}[1,1'-biphenyl]-4-carboxamideHCID 1843605813.5%

반응 단계

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.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07183415B2
출처 데이터셋uspto-grants-2007_02
ORD IDord-51f39c8bf894482a9608cf77ec3a671b
출처 메모uspto-grants-2007_02