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Lithium Hydroxide → 2-Oxo-1,2-dihydro-1,7-naphthyridine-3-carboxylic acid

HRID 525391
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HRID 525391 반응식
[O:1]=[C:2]1[C:11]([C:12]([O:14]C)=[O:13])=[CH:10][C:9]2[C:4](=[CH:5][N:6]=[CH:7][CH:8]=2)[NH:3]1.[OH-].[Li+]>C1COCC1.O>[O:1]=[C:2]1[C:11]([C:12]([OH:14])=[O:13])=[CH:10][C:9]2[C:4](=[CH:5][N:6]=[CH:7][CH:8]=2)[NH:3]1
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참가 물질

5

반응물 2

HCID 3939Lithium HydroxideHCID 46835264Methyl 2-hydroxy-1,7-naphthyridine-3-carboxylate

생성물 1

HCID 184040862-Oxo-1,2-dihydro-1,7-naphthyridine-3-carboxylic acid수율 89%

시약·촉매·용매 2

HCID 962Water용매HCID 8028Tetrahydrofuran용매

반응 조건

온도
65 °C

실험 절차

A mixture of methyl 2-oxo-1,2-dihydro-1,7-naphthyridine-3-carboxylate (prepared as described in WO 2010/016846)(4.22 g, 20.67 mmol) and lithium hydroxide (2.475 g, 103 mmol) in THF (50 mL) and water (50 mL) was heated at 65° C. for 1 hour. The white precipitate was filtered, washed with water, and dried to afford a white solid. The filtrate was concentrated, dissolved in water and neutralized to pH=7 with concentrated HCl to afford a white solid. The white precipitate was filtered, washed with water, and dried. The solids were combined to afford 2-oxo-1,2-dihydro-1,7-naphthyridine-3-carboxylic acid (3.482 g, 18.31 mmol, 89% yield) as an off-white solid. m/z (ESI) 191.2 (M+H)+.

후처리

  1. filtrationThe white precipitate was filtered
  2. washwashed with water
  3. customdried
  4. customto afford a white solid
  5. concentrationThe filtrate was concentrated
  6. dissolutiondissolved in water and neutralized to pH=7 with concentrated HCl
  7. customto afford a white solid
  8. filtrationThe white precipitate was filtered
  9. washwashed with water
  10. customdried

출처 및 근거

ORD 기록
ord-0cb91b6113f74dc5b7161456ab876378
출처 데이터셋
uspto-grants-2016_05
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US09340549B2

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