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Methanol → 7-Methoxyquinoline-3-carboxylic acid

HRID 1865423
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인쇄 미리보기

반응식

HRID 1865423 반응식
[CH3:1][O:2][C:3]1[CH:12]=[C:11]2[C:6]([CH:7]=[C:8]([C:13]([O:15]CC)=[O:14])[CH:9]=[N:10]2)=[CH:5][CH:4]=1.CO.[OH-].[Na+]>C1COCC1>[CH3:1][O:2][C:3]1[CH:12]=[C:11]2[C:6]([CH:7]=[C:8]([C:13]([OH:15])=[O:14])[CH:9]=[N:10]2)=[CH:5][CH:4]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 887MethanolHCID 14798Sodium HydroxideHCID 21865246Ethyl 7-methoxyquinoline-3-carboxylate

생성물 1

HCID 146728247-Methoxyquinoline-3-carboxylic acid

시약·촉매·용매 1

HCID 8028Tetrahydrofuran용매

실험 절차

To a solution of the intermediate from step C (399 mg, mmol) in THF (6 mL) was added methanol (1 mL) followed by NaOH (5N, 1.5 mL). After stirring at room temperature for 18 hours the reaction was concentrated in vacuo. The residue was acidified with 1N HCl (10 mL). The solution was concentrated in vacuo and azeotroped with toluene (4×). This material was used in the next step without any further purification.

후처리

  1. concentrationwas concentrated in vacuo
  2. concentrationThe solution was concentrated in vacuo
  3. customazeotroped with toluene (4×)
  4. customThis material was used in the next step without any further purification

출처 및 근거

ORD 기록
ord-22146aec56cb4f5692070cd8f65af8cd
출처 데이터셋
uspto-grants-2009_12
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07625938B2

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