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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1887781생성일: 2026년 10월 27일

Sodium bis(trimethylsilyl)amide → 7-chloro-3-methyl-2-oxazol-2-yl-1-phenyl-1H-quinolin-4-one

https://huagongshe.com/reaction/1887781

반응식

참여 물질

역할이름HCID투입량
반응물Sodium bis(trimethylsilyl)amideHCID 2724254—
반응물Oxazole-2-carbonyl chlorideHCID 22646749—
반응물1-(4-Chloro-2-phenylamino-phenyl)-propan-1-oneHCID 70816614—
촉매DimethylformamideHCID 6228—
용매TetrahydrofuranHCID 8028—
생성물7-chloro-3-methyl-2-oxazol-2-yl-1-phenyl-1H-quinolin-4-oneHCID 7120819023.6%

반응 단계

In a 25 mL round-bottomed flask, 1-(4-chloro-2-phenylamino-phenyl)-propan-1-one (522 mg, 2.01 mmol) was combined with THF (4 mL) to give a yellow solution. Sodium bis(trimethylsilyl)amide (1.0 M in THF) (5.02 mL, 5.02 mmol) was added slowly dropwise, resulting in a dark red solution. A mixture of oxazole-2-carbonyl chloride (344 mg, 2.61 mmol) in THF (8 mL) and 8 drops of DMF were added to the reaction mixture. The resulting mixture was stirred at room temperature for 5 hr. The reaction mixture was quenched by the addition of water and the aqueous layer was extracted with ethyl acetate. The organic phase was dried (MgSO4), filtered, then concentrated to afford a yellow oil. The crude material was purified by flash chromatography (silica gel, 80 g, 25-65% ethyl acetate in hexanes) to give 7-chloro-3-methyl-2-oxazol-2-yl-1-phenyl-1H-quinolin-4-one (160 mg, 23.6%) as a yellowish solid. MS calcd. for C19H13ClN2O2 [(M+H)+] 337, obsd. 337.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08501732B2
출처 데이터셋uspto-grants-2013_08
ORD IDord-927e09f4728c4fddaa2a5b8fde1b9c2d
출처 메모uspto-grants-2013_08