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Dimethylformamide → [(6-Nitro-5-quinolinyl)amino]oxo-acetic acid ethyl ester

HRID 48232
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인쇄 미리보기

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HRID 48232 반응식
[NH2:1][C:2]1[C:11]([N+:12]([O-:14])=[O:13])=[CH:10][CH:9]=[C:8]2[C:3]=1[CH:4]=[CH:5][CH:6]=[N:7]2.C(N([CH2:20][CH3:21])CC)C.CC[C:24]([C:26](Cl)=[O:27])=[O:25].CN(C)C=[O:32]>>[CH2:20]([O:32][C:24](=[O:25])[C:26]([NH:1][C:2]1[C:11]([N+:12]([O-:14])=[O:13])=[CH:10][CH:9]=[C:8]2[C:3]=1[CH:4]=[CH:5][CH:6]=[N:7]2)=[O:27])[CH3:21]
참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 4

HCID 6228DimethylformamideHCID 8471TriethylamineHCID 1189016-Nitroquinolin-5-ylamineHCID 11007880Butanoyl chloride, 2-oxo-

생성물 1

HCID 10085554[(6-Nitro-5-quinolinyl)amino]oxo-acetic acid ethyl ester수율 80%

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온도
50 °C

실험 절차

A solution of 5-amino-6-nitroquinoline (3 g, 16 mmol) in 50 mL dimethylformamide was treated with triethylamine (3.2 g, 32 mmol) and ethyloxalyl chloride (3.2 g, 24 mmol) and heated at 50° C. for 1 hour. After removing the triethylamine hydrochloride by filtration, the filtrate was concentrated and diethyl ether added. The title compound (3.7 g, 80% yield) was collected by filtration.

후처리

  1. customAfter removing the triethylamine hydrochloride
  2. filtrationby filtration
  3. concentrationthe filtrate was concentrated
  4. additiondiethyl ether added

출처 및 근거

ORD 기록
ord-a11dfcfbd646463ca3727e7a64b8193d
출처 데이터셋
uspto-grants-2004_03
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US06703391B2

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