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
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Sodium bis(trimethylsilyl)amide | HCID 2724254 | — |
| 반응물 | Oxazole-2-carbonyl chloride | HCID 22646749 | — |
| 반응물 | 1-(4-Chloro-2-phenylamino-phenyl)-propan-1-one | HCID 70816614 | — |
| 촉매 | Dimethylformamide | HCID 6228 | — |
| 용매 | Tetrahydrofuran | HCID 8028 | — |
| 생성물 | 7-chloro-3-methyl-2-oxazol-2-yl-1-phenyl-1H-quinolin-4-one | HCID 71208190 | 23.6% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US08501732B2 |
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| 출처 데이터셋 | uspto-grants-2013_08 |
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| ORD ID | ord-927e09f4728c4fddaa2a5b8fde1b9c2d |
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| 출처 메모 | uspto-grants-2013_08 |
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