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

HRID 82231
ノート
印刷プレビュー

反応式

HRID 82231 の反応式
[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
参加物反応条件実験手順後処理出典と根拠反応ノート

参加物

5

反応物 3

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

生成物 1

HCID 866721091,5-Naphthyridin-3-ylacetic acid

試薬・触媒・溶媒 1

HCID 312751,4-Dioxane溶媒

反応条件

温度
100 °C

実験手順

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.

このページの内容参加物反応条件実験手順後処理出典と根拠反応ノート

後処理

  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

出典と根拠

ORDレコード
ord-8cc1783b27924989bf2dfc628360f3b9
出典データセット
uspto-grants-2014_09
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US08846698B2

反応ノート

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