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Hydrochloric Acid → 1,5-Naphthyridin-3-ylacetic acid

HRID 82231
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HRID 82231 반응식
[OH-].[Na+].[N:3]1[C:12]2[C:7](=[N:8][CH:9]=[CH:10][CH:11]=2)[CH:6]=[C:5]([CH2:13][C:14]([O:16]CC)=[O:15])[CH:4]=1.Cl>O1CCOCC1>[N:3]1[C:12]2[C:7](=[N:8][CH:9]=[CH:10][CH:11]=2)[CH:6]=[C:5]([CH2:13][C:14]([OH:16])=[O:15])[CH:4]=1
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참가 물질

5

반응물 3

HCID 313Hydrochloric AcidHCID 14798Sodium HydroxideHCID 70817520Ethyl 1,5-naphthyridin-3-ylacetate

생성물 1

HCID 866721091,5-Naphthyridin-3-ylacetic acid

시약·촉매·용매 1

HCID 312751,4-Dioxane용매

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온도
100 °C

실험 절차

Sodium hydroxide (10 mL, 2.0 M) was added to ethyl 1,5-naphthyridin-3-ylacetate in 1,4-dioxane (10 mL) and the mixture was heated at 100° C. for 6 hours. The reaction mixture was cooled to room temperature and acidified to pH 4 using aqueous 2M HCl and then evaporated in vacuo. The residue was azeotroped with toluene (2×15 mL) then dissolved in THF (50 mL) and stirred at 40° C. for 30 min. The mixture was filtered, the filtrate was evaporated in vacuo and the residue was triturated with diethyl ether to afford the title compound as an off white solid, 200 mg.

후처리

  1. temperatureThe reaction mixture was cooled to room temperature
  2. customevaporated in vacuo
  3. customThe residue was azeotroped with toluene (2×15 mL)
  4. dissolutionthen dissolved in THF (50 mL)
  5. filtrationThe mixture was filtered
  6. customthe filtrate was evaporated in vacuo
  7. customthe residue was triturated with diethyl ether

출처 및 근거

ORD 기록
ord-8cc1783b27924989bf2dfc628360f3b9
출처 데이터셋
uspto-grants-2014_09
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08846698B2

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