돌아가기
Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 40324생성일: 2026년 10월 23일

Oxalyl chloride → N-Methoxy-N-methylquinoline-6-carboxamide

https://huagongshe.com/ko/reaction/40324

반응식

참여 물질

역할이름HCID투입량
반응물Oxalyl chlorideHCID 65578—
반응물Methanamine, N-methoxy-, hydrochloride (1:1)HCID 81138—
반응물DiisopropylethylamineHCID 81531—
반응물6-Quinolinecarboxylic acidHCID 82571—
촉매DimethylformamideHCID 6228—
용매DichloromethaneHCID 6344—
생성물N-Methoxy-N-methylquinoline-6-carboxamideHCID 5521117295.2%

반응 단계

A 250 mL RB flask was charged with quinoline-6-carboxylic acid (5.00 g, 28.9 mmol), DCM (100 ml, 1554 mmol), oxalyl chloride (3.79 ml, 43.3 mmol), and a few drops of DMF and stirred at RT for 2 hours, then concentrated. The residue was taken up in DCM (100 ml, 1554 mmol), cooled to 0° C., then Hunig's Base (17.7 ml, 101 mmol) and N-methoxymethanamine hydrochloride (2.96 g, 30.3 mmol) were added slowly. The mixture was stirred at room temperature for 16 hours (91463-3-1). The mixture was diluted with DCM (200 mL), then washed with water (250 mL), sat. NaHCO3 (250 mL), and brine (250 mL). The organic layer was dried with MgSO4, filtered, and concentrated to give a brown oil, which was purified by MPLC eluting with 2-6% MeOH/DCM to give N-methoxy-N-methylquinoline-6-carboxamide (5.943 g, 95.2% yield) as a brown oil.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08524900B2
출처 데이터셋uspto-grants-2013_09
ORD IDord-1c22e723dddd4c25b16eeb5f4c0677ad
출처 메모uspto-grants-2013_09