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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 2212191생성일: 2026년 10월 25일

Potassium bis(trimethylsilyl)amide → 3-(9-chloro-3-methyl-4-oxo-5H-isoxazolo[4,3-c]quinolin-5-yl)-piperidine-1-carboxylic acid methyl ester

https://huagongshe.com/reaction/2212191

반응식

참여 물질

역할이름HCID투입량
반응물Potassium bis(trimethylsilyl)amideHCID 3251421—
반응물3-{[3-(2-Chloro-6-fluoro-phenyl)-5-methyl-isoxazole-4-carbonyl]-amino}-piperidine-1-carboxylic acid methyl esterHCID 69652389—
용매DimethylformamideHCID 6228—
생성물3-(9-chloro-3-methyl-4-oxo-5H-isoxazolo[4,3-c]quinolin-5-yl)-piperidine-1-carboxylic acid methyl esterHCID 995156192.4%

반응 단계

Add potassium bis(trimethylsilyl)-amide (5.5 mL, 2.73 mmol, 0.5 M in toluene) to a solution of 3-{[3-(2-chloro-6-fluoro-phenyl)-5-methyl-isoxazole-4-carbonyl]-amino}-piperidine-1-carboxylic acid methyl ester (0.72 g, 1.82 mmol) in dimethylformamide (56 mL). After 5 minutes, quench the reaction with 1N HCl and concentrate. Partition the resulting material between 20% isopropanol/chloroform and 1N HCl. Wash the organic layer with saturated aqueous sodium bicarbonate solution and brine, dry over magnesium sulfate, and concentrate. Purify by flash chromatography on silica gel (eluting with 0–0.5% methanol/chloroform) to give 632 mg of the title compound as a white solid, 92% yield. 1H NMR: consistent with structure. MS (ion spray) 376 (M+).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07101891B2
출처 데이터셋uspto-grants-2006_09
ORD IDord-98d59a58ccf449549ce5dfcde00cd7cb
출처 메모uspto-grants-2006_09