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llms.txt · MCP 가이드개인정보처리방침 · 이용약관 · 지원v1.8.0
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Ethyl 4-(5,6,7,8-tetrahydro-1,8-naphthyridin-2-yl)butanoate → 4-(5,6,7,8-Tetrahydro-1,8-naphthyridin-2-yl)butanoic acid

HRID 1761037
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인쇄 미리보기

반응식

HRID 1761037 반응식
[N:1]1[C:10]2[NH:9][CH2:8][CH2:7][CH2:6][C:5]=2[CH:4]=[CH:3][C:2]=1[CH2:11][CH2:12][CH2:13][C:14]([O:16]CC)=[O:15]>Cl>[N:1]1[C:10]2[NH:9][CH2:8][CH2:7][CH2:6][C:5]=2[CH:4]=[CH:3][C:2]=1[CH2:11][CH2:12][CH2:13][C:14]([OH:16])=[O:15]
참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트

참가 물질

3

반응물 1

HCID 22594332Ethyl 4-(5,6,7,8-tetrahydro-1,8-naphthyridin-2-yl)butanoate

생성물 1

HCID 154622344-(5,6,7,8-Tetrahydro-1,8-naphthyridin-2-yl)butanoic acid

시약·촉매·용매 1

HCID 313Hydrochloric Acid용매

반응 조건

온도
55 °C

실험 절차

The ester obtained in Step b (0.36 g; 1.45 mmol) is dissolved in 10 ml of 6N HCl. The reaction mixture is heated at 55° C. for 4 hours. The reaction mixture is then concentrated, and the residue is taken up in AcOEt. The resulting precipitate, corresponding to the title product, is suction-filtered off over a frit and isolated in the form of a pale yellow solid.

후처리

  1. concentrationThe reaction mixture is then concentrated
  2. filtrationThe resulting precipitate, corresponding to the title product, is suction-filtered off over a frit
  3. customisolated in the form of a pale yellow solid

출처 및 근거

ORD 기록
ord-d3017aeab6e24f4faa34700fa15ce092
출처 데이터셋
uspto-grants-2005_01
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US06846833B2

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