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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 48910생성일: 2026년 10월 23일

Dimethylformamide → Ethyl 8-Azido-4-Oxo-4H-Quinolizine-3-Carboxylate

https://huagongshe.com/ko/reaction/48910

반응식

참여 물질

역할이름HCID투입량
반응물DimethylformamideHCID 6228—
반응물Sodium AzideHCID 33557—
반응물Ethyl 8-chloro-4-oxo-4H-quinolizine-3-carboxylateHCID 3314858—
용매WaterHCID 962—
생성물Ethyl 8-Azido-4-Oxo-4H-Quinolizine-3-CarboxylateHCID 2063415785%

반응 조건

온도40 °C

반응 단계

An oven-dried 25 ml round-bottom flask was purged with argon and charged with ethyl 8-chloro-4-oxo-4H-quinolizine-3-carboxylate (2) (250 mg, 1 mmol), NaN3 (300 mg, 4.6 mmol), and 5 ml DMF. The reaction mixture was stirred at 40° C. for 1 h, cooled to room temperature, and poured into 100 ml water. The aqueous layer was extracted three times with 100 ml chloroform, and the combined organic layers were washed three times with 100 ml water. The organic solvent was evaporated and the crude product was purified by flash chromatography (ethyl acetate) to give a deep red crystalline solid (218 mg, 85%). M.p. 145-150° C. 1H NMR (δ, CDCl3): 1.42 (t, J=7 Hz, 3H), 4.41 (q, J=7 Hz, 2H), 6.53 (d, J=8 Hz, 1H), 6.84 (dd, J=2 Hz, J=7 Hz, 1H), 7.08 (d, J=2 Hz, 1H), 8.37 (d, J=8 Hz, 1H), 9.36 (d, J=7 Hz, 1H). MS: m/z 258.0751; required for C12H10N4O3: 258.0753.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06706528B2
출처 데이터셋uspto-grants-2004_03
ORD IDord-00124a126b114070a4139697ee5b43e7
출처 메모uspto-grants-2004_03