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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 992560생성일: 2026년 10월 27일

Sodium hydride → methyl 9-(2,5-dichlorobenzyl)-9H-beta-carboline-3-carboxylate

https://huagongshe.com/reaction/992560

반응식

참여 물질

역할이름HCID투입량
반응물Sodium hydrideHCID 24758—
반응물Beta-CarbolineHCID 64961—
반응물2,5-Dichlorobenzyl chlorideHCID 75976—
반응물Methyl 9H-pyrido(3,4-b)indole-3-carboxylateHCID 107704—
반응물SodiumHCID 5360545—
용매WaterHCID 962—
용매DimethylformamideHCID 6228—
생성물methyl 9-(2,5-dichlorobenzyl)-9H-beta-carboline-3-carboxylateHCID 990812288%

반응 단계

To a suspension of sodium hydride (1.60 g of 60% dispersion in oil, 0.04 mol) in dry DMF (60 mL) was added methyl 9H-β-carboline-3-carboxylate (8.7 g, 0.0385 mol) at −20° C. with stirring. The mixture was allowed to warm to room temperature with stirring under nitrogen. After stirring for 10 minutes at room temperature, formation of the sodium salt of the β-carboline appeared to be complete, resulting in a clear brown solution. The reaction mixture was cooled in an ice bath, 2,5-dichlorobenzyl chloride (7.82 g, 0.040 mol) was added, and the mixture was allowed to warm to room temperature and stirred overnight. The reaction mixture was diluted with water (200 mL), filtered, and the cake washed with water, ethyl acetate, ether, and dried, affording 13.05 g (88%) of the title product. 1H NMR (CDCl3) δ8.88 (s, 1H), 8.78 (s, 1H), 8.20 (d, J=7.8 Hz, 1H), 7.61 (t, J=7.8 Hz, 1H), 7.45-7.35 (m, 3H) 7.18 (dd, J=8.2, 1.7 Hz,1H), 6.52 (s, 1H), 5.56 (s, 2H), 4.06 (s, 3H); MS (APCI; (M+H)+) m/z 385.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06469021B1
출처 데이터셋uspto-grants-2002_10
ORD IDord-d9f8c7acaab742b78147fe775900c25b
출처 메모uspto-grants-2002_10