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Sulfuric Acid → 6,7-Dimethoxyisoquinolin-3-amine

HRID 1876026
ノート
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反応式

HRID 1876026 の反応式
[CH3:1][O:2][C:3]1[CH:4]=[C:5]([CH:17]=[CH:18][C:19]=1[O:20][CH3:21])[CH2:6][NH:7][C:8](=[NH:16])[CH:9](OCC)OCC.S(=O)(=O)(O)O.[OH-].[Na+]>>[CH3:21][O:20][C:19]1[CH:18]=[C:17]2[C:5](=[CH:4][C:3]=1[O:2][CH3:1])[CH:6]=[N:7][C:8]([NH2:16])=[CH:9]2
参加物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 1118Sulfuric AcidHCID 14798Sodium HydroxideHCID 178471678HCID 178471678、化合物

生成物 1

HCID 233211636,7-Dimethoxyisoquinolin-3-amine

実験手順

To N-(3,4-dimethoxybenzyl)-2,2-diethoxyacetimidamide (541 mg, 1.825 mmol) was added sulfuric acid (0.95 mL, 1.825 mmol) was added. After cooling, the reaction was allowed to stand at ambient temperature overnight. It was added dropwise to ice, then the resulting solution was neutralized with conc. NaOH, and the aqueous phase was twice extracted with ethyl acetate. The combined ethyl acetate fractions were dried over magnesium sulfate. The drying agent was filtered off and the solvent evaporated. The residue was purified by column chromatography in 5% methanol/ethyl acetate, collecting the main component. Yield 105.7 mg brown solid (28%).

後処理

  • additionwas added
  • temperatureAfter cooling
  • additionIt was added dropwise to ice
  • extractionthe aqueous phase was twice extracted with ethyl acetate
  • dry with materialThe combined ethyl acetate fractions were dried over magnesium sulfate
  • filtrationThe drying agent was filtered off
  • customthe solvent evaporated
  • customThe residue was purified by column chromatography in 5% methanol/ethyl acetate
  • customcollecting the main component
  • 出典と根拠

    ORDレコード
    ord-a4913968c26f45ddbb3ed2629a6b6cf2
    出典データセット
    uspto-grants-2012_11
    DOI
    10.6084/m9.figshare.5104873.v1
    特許番号
    US08309577B2

    反応ノート

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