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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 33821생성일: 2026년 10월 24일

Triethylamine → Benzamide, N-methoxy-N-methyl-4-(2-quinolinylmethoxy)-

https://huagongshe.com/ko/reaction/33821

반응식

참여 물질

역할이름HCID투입량
반응물TriethylamineHCID 8471—
반응물Methanamine, N-methoxy-, hydrochloride (1:1)HCID 81138—
반응물4-(quinolin-2-ylmethoxy)benzoic AcidHCID 9838552—
용매Thionyl ChlorideHCID 24386—
생성물Benzamide, N-methoxy-N-methyl-4-(2-quinolinylmethoxy)-HCID 44234674—

반응 단계

To a solution of 4-(Quinolin-2-ylmethoxy)-benzoic acid (25.98 g, 93 mmole) was added 250 ml of thionyl chloride under N2. The reaction mixture stirred 3 h and the excess thionyl chloride was removed under vacuum. The acid chloride was dissolved in tetrahydrofuran (450 ml) and triethylamine (50 ml, 4 eq.) was slowly added. O,N-dimethyl hydroxyl amine hydrochloride (27 g, 3 eq.) was added and the reaction stirred 18 h. The reaction mixture was placed on a rotovap to remove the solvent, partitioned between 1N NaOH and methylene chloride, separated, dried magnesium sulfate, filtered and concentrated. The crude product was filtered through silica gel eluting with 30-70% ethyl acetate/hexane to proved the title compound as a brown oil (26.26 g, 87%); 1H NMR (400 MHz, CDCl3) δ 8.17 (d, J=8.7 Hz, 1 H), 8.06 (d, J=8.3 Hz, 1 H), 7.81 (d, J=8.3 Hz, 1H), 7.67 (m, 3 H), 7.63 (d, J=8.3 Hz, 1 H), 7.52 (m, 1 H), 7.01 (M, 2 H), 5.39 (s, 2 H), 3.52 (s, 3 H) 3.31 (s, 2H); MS: (M+H m/z=323.2).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07429665B2
출처 데이터셋uspto-grants-2008_09
ORD IDord-aa182ead62ca49b9b1b7f0453dac61ec
출처 메모uspto-grants-2008_09