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Nitric Acid → 5-Bromo-8-ethoxalylamino-7-nitroquinoline

HRID 48230
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인쇄 미리보기

반응식

HRID 48230 반응식
[CH2:1]([O:3][C:4](=[O:19])[C:5]([NH:7][C:8]1[CH:9]=[CH:10][C:11]([Br:18])=[C:12]2[C:17]=1[N:16]=[CH:15][CH:14]=[CH:13]2)=[O:6])[CH3:2].[N+:20]([O-])([OH:22])=[O:21]>FC(F)(F)C(O)=O>[CH2:1]([O:3][C:4](=[O:19])[C:5]([NH:7][C:8]1[C:9]([N+:20]([O-:22])=[O:21])=[CH:10][C:11]([Br:18])=[C:12]2[C:17]=1[N:16]=[CH:15][CH:14]=[CH:13]2)=[O:6])[CH3:2]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 944Nitric AcidHCID 47744235-Bromo-8-ethoxalylaminoquinoline

생성물 1

HCID 117264985-Bromo-8-ethoxalylamino-7-nitroquinoline수율 45%

시약·촉매·용매 1

HCID 6422Trifluoroacetic acid용매

실험 절차

A solution of the product from Example 82 (23.5 g, 58 mmol) in 30 mL fuming nitric acid and 150 mL trifluoroacetic acid was heated at 80° C. for 18 hours. The solvent was removed and the residue was treated with water to give a solid. The solid was collected by filtration and washed with ether and dried to give the title compound (9.5 g, 45% yield).

후처리

이 페이지에서참가 물질실험 절차후처리출처 및 근거반응 노트
  1. customThe solvent was removed
  2. additionthe residue was treated with water
  3. customto give a solid
  4. filtrationThe solid was collected by filtration
  5. washwashed with ether
  6. customdried

출처 및 근거

ORD 기록
ord-a9da6a8a18414bbcb6b8c0cdc89508a7
출처 데이터셋
uspto-grants-2004_03
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US06703391B2

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