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

HRID 1876026
Notizen
Druckvorschau

Reaktionsgleichung

Reaktionsgleichung von HRID 1876026
[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
KomponentenVersuchsvorschriftAufarbeitungQuellen und NachweiseNotizen zur Reaktion

Komponenten

4

Edukt 3

HCID 1118Sulfuric AcidHCID 14798Sodium HydroxideHCID 178471678HCID 178471678, Verbindung

Produkt 1

HCID 233211636,7-Dimethoxyisoquinolin-3-amine

Versuchsvorschrift

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%).

Aufarbeitung

  1. additionwas added
  2. temperatureAfter cooling
  3. additionIt was added dropwise to ice
  4. extractionthe aqueous phase was twice extracted with ethyl acetate
  5. dry with materialThe combined ethyl acetate fractions were dried over magnesium sulfate
  6. filtrationThe drying agent was filtered off
  7. customthe solvent evaporated
  8. customThe residue was purified by column chromatography in 5% methanol/ethyl acetate
  9. customcollecting the main component

Quellen und Nachweise

ORD-Eintrag
ord-a4913968c26f45ddbb3ed2629a6b6cf2
Quelldatensatz
uspto-grants-2012_11
DOI
10.6084/m9.figshare.5104873.v1
Patentnummer
US08309577B2

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