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Sodium Hydroxide → 2-(2-oxo-1,5-naphthyridin-1(2H)-yl)acetic acid

HRID 1519792
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인쇄 미리보기

반응식

HRID 1519792 반응식
[O:1]=[C:2]1[CH:11]=[CH:10][C:9]2[C:4](=[CH:5][CH:6]=[CH:7][N:8]=2)[N:3]1[CH2:12][C:13]([O:15]C)=[O:14].[OH-].[Na+]>C1COCC1>[O:1]=[C:2]1[CH:11]=[CH:10][C:9]2[C:4](=[CH:5][CH:6]=[CH:7][N:8]=2)[N:3]1[CH2:12][C:13]([OH:15])=[O:14]
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참가 물질

4

반응물 2

HCID 14798Sodium HydroxideHCID 68782636methyl 2-(2-oxo-1,5-naphthyridin-1(2H)-yl)acetate

생성물 1

HCID 687824352-(2-oxo-1,5-naphthyridin-1(2H)-yl)acetic acid

시약·촉매·용매 1

HCID 8028Tetrahydrofuran용매

반응 조건

온도
70 °C

실험 절차

To a solution of methyl 2-(2-oxo-1,5-naphthyridin-1(2H)-yl)acetate (0.205 g, 0.939 mmol) in THF (5 mL) was added sodium hydroxide (0.939 mL of a 3 N aqueous solution, 2.818 mmol) and the reaction mixture was stirred at 70° C. for 0.5 h. The resulting solution was concentrated under vacuum and co-evaporated from toluene to give 2-(2-oxo-1,5-naphthyridin-1(2H)-yl)acetic acid. Retention time (min)=1.033, method [3], MS(ESI) 205.1 (M+H).

후처리

  1. concentrationThe resulting solution was concentrated under vacuum

출처 및 근거

ORD 기록
ord-4e8221493cb346fbba44b797e2e691c2
출처 데이터셋
uspto-grants-2015_07
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US09073891B2

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