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Diethyl Malonate → Ethyl 6-nitro-2-oxo-1,2-dihydroquinoline-3-carboxylate

HRID 1995334
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인쇄 미리보기

반응식

HRID 1995334 반응식
[NH2:1][C:2]1[CH:9]=[CH:8][C:7]([N+:10]([O-:12])=[O:11])=[CH:6][C:3]=1[CH:4]=O.[C:13](OCC)(=[O:20])[CH2:14][C:15]([O:17][CH2:18][CH3:19])=[O:16]>>[N+:10]([C:7]1[CH:6]=[C:3]2[C:2](=[CH:9][CH:8]=1)[NH:1][C:13](=[O:20])[C:14]([C:15]([O:17][CH2:18][CH3:19])=[O:16])=[CH:4]2)([O-:12])=[O:11]
참가 물질실험 절차출처 및 근거반응 노트

참가 물질

3

반응물 2

HCID 7761Diethyl MalonateHCID 2792602-Amino-5-nitrobenzaldehyde

생성물 1

HCID 13106328Ethyl 6-nitro-2-oxo-1,2-dihydroquinoline-3-carboxylate

실험 절차

A solution of 10.0 g (46 mmol) of 1,2-dihydro-2-oxo-3-quinolinecarboxylic acid, ethyl ester [J. Chem. Soc., 2518 (1962)] and 50 ml of sulfuric acid is stirred in an ice bath and a cold mixture of 9.75 ml of 70% nitric acid and 9.75 ml of sulfuric acid is added dropwise over 10 minutes. The reaction solution is stirred with ice bath cooling for 1 hour and then is poured into ice and water with stirring. The resulting solid is collected by filtration and washed with water and ethanol. After drying, 10.7 g of the requisite ester is obtained, mp>310° C. The structure is assigned by an unequivocal synthesis from the condensation of 2-amino-5-nitro-benzaldehyde and diethyl malonate to give the same 1,2-dihydro-6-nitro-2-oxo-3-quinolinecarboxylic acid, ethyl ester.

출처 및 근거

ORD 기록
ord-83ec0c9c0647415ca45744c4644d9422
출처 데이터셋
uspto-grants-1983_09
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04404201

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