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llms.txt · MCP 가이드개인정보처리방침 · 이용약관 · 지원v1.8.0
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(1-Ethyl-7-methoxy-2-oxo-1,2-dihydro-quinolin-3-yl)-acetic acid methyl ester → (1-Ethyl-7-hydroxy-2-oxo-1,2-dihydro-quinolin-3-yl)-acetic Acid

HRID 2301974
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인쇄 미리보기

반응식

HRID 2301974 반응식
C[O:2][C:3](=[O:20])[CH2:4][C:5]1[C:6](=[O:19])[N:7]([CH2:17][CH3:18])[C:8]2[C:13]([CH:14]=1)=[CH:12][CH:11]=[C:10]([O:15]C)[CH:9]=2>Br.CC(O)=O>[CH2:17]([N:7]1[C:8]2[C:13](=[CH:12][CH:11]=[C:10]([OH:15])[CH:9]=2)[CH:14]=[C:5]([CH2:4][C:3]([OH:20])=[O:2])[C:6]1=[O:19])[CH3:18]
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참가 물질

3

반응물 1

HCID 69978872(1-Ethyl-7-methoxy-2-oxo-1,2-dihydro-quinolin-3-yl)-acetic acid methyl ester

생성물 1

HCID 18462610(1-Ethyl-7-hydroxy-2-oxo-1,2-dihydro-quinolin-3-yl)-acetic Acid수율 89.3%

시약·촉매·용매 1

HCID 21893785Acetic Acid Mixture with Hydrobromic Acid용매

반응 조건

온도
250 °C

실험 절차

A suspension of (1-ethyl-7-methoxy-2-oxo-1,2-dihydro-quinolin-3-yl)-acetic acid methyl ester (4.0 g, 14.5 mmol) in 1:1 48% aqueous HBr—HOAc (30 mL) was heated at reflux for 48 h. The resulting solution was cooled to 250° C. and the resulting crystalline solid was stored at 0-50° C. for 2 h, then vacuum filtered, washed with water and air-dried to give the title compound (3.2 g, 89% yield) as tan needles.

후처리

  1. temperaturewas heated
  2. temperatureat reflux for 48 h
  3. filtrationvacuum filtered
  4. washwashed with water
  5. customair-dried

출처 및 근거

ORD 기록
ord-b3815e8571724cc881df994841c75bd6
출처 데이터셋
uspto-grants-2002_08
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US06429214B1

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