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Phosphorus oxychloride → HCID 58577766、化合物

HRID 1430051
ノート
印刷プレビュー

反応式

HRID 1430051 の反応式
O=[C:2]1[N:10]([CH2:11][C:12]([O:14][CH2:15][CH3:16])=[O:13])[C:5]2=[N:6][CH:7]=[CH:8][CH:9]=[C:4]2[NH:3]1.C(=O)(O)[O-].[Na+].P(Cl)(Cl)([Cl:24])=O>>[Cl:24][C:2]1[N:10]([CH2:11][C:12]([O:14][CH2:15][CH3:16])=[O:13])[C:5]2=[N:6][CH:7]=[CH:8][CH:9]=[C:4]2[N:3]=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

4

反応物 3

HCID 24813Phosphorus oxychlorideHCID 516892Sodium BicarbonateHCID 67335103ethyl 2-(2-oxo-1H-imidazo[4,5-b]pyridin-3(2H)-yl)acetate

生成物 1

HCID 58577766HCID 58577766、化合物

反応条件

温度
100 °C

実験手順

A mixture of ethyl (2-oxo-1,2-dihydro-3H-imidazo[4,5-b]pyridin-3-yl)acetate (14.5 g) and phosphoryl chloride (100 mL) was stirred at 100° C. overnight. The mixture was poured into ice, neutralized with saturated sodium bicarbonate solution and extracted with AcOEt. The organic layer was dried over Na2SO4, filtered and concentrated under reduced pressure. The residue was diluted with AcOEt and insoluble crystals were removed by filtration. The filtrate was concentrated under reduced pressure. The residue was purified by column chromatography (silica gel, eluted with 10%-40% AcOEt in hexane) to give the title compound (5.46 g).

後処理

  1. additionThe mixture was poured into ice
  2. extractionextracted with AcOEt
  3. dry with materialThe organic layer was dried over Na2SO4
  4. filtrationfiltered
  5. concentrationconcentrated under reduced pressure
  6. additionThe residue was diluted with AcOEt and insoluble crystals
  7. customwere removed by filtration
  8. concentrationThe filtrate was concentrated under reduced pressure
  9. customThe residue was purified by column chromatography (silica gel, eluted with 10%-40% AcOEt in hexane)

出典と根拠

ORDレコード
ord-6f59942429a94a0891b912961d0383a3
出典データセット
uspto-grants-2015_01
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US08940758B2

反応ノート

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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