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Hydrochloric Acid → HCID 20183601, Verbindung

HRID 255536
Notizen
Druckvorschau

Reaktionsgleichung

Reaktionsgleichung von HRID 255536
[ClH:1].[NH2:2][C:3]1[CH:4]=[N:5][C:6]2[C:11]([C:12]=1[NH:13][CH3:14])=[CH:10][C:9]([CH3:15])=[CH:8][CH:7]=2.[C:16]([OH:20])(=O)[CH2:17][OH:18].Cl.[OH-].[Na+]>>[OH2:18].[ClH:1].[CH3:14][N:13]1[C:12]2[C:11]3[CH:10]=[C:9]([CH3:15])[CH:8]=[CH:7][C:6]=3[N:5]=[CH:4][C:3]=2[N:2]=[C:17]1[CH2:16][OH:20]
KomponentenVersuchsvorschriftAufarbeitungQuellen und NachweiseNotizen zur Reaktion

Komponenten

5

Edukt 4

HCID 313Hydrochloric AcidHCID 757Glycolic AcidHCID 14798Sodium HydroxideHCID 13958355HCID 13958355, Verbindung

Produkt 1

HCID 20183601HCID 20183601, Verbindung

Versuchsvorschrift

A mixture of 4.5 g (0.020 mole) of 3-amino-6-methyl-4-(methylamino)quinoline hydrochloride (from Example 32), 3.8 g (0.050 mole) of glycolic acid and 75 ml of 4 N hydrochloric acid was heated at its reflux temperature for two hours. The solution was cooled, and 50% aqueous sodium hydroxide was then added to make the solution slightly basic. The precipitate was separated by filtration and washed with water. The solid was redissolved in dilute hydrochloric acid and reprecipitated with ammonium hydroxide to provide 1,8-dimethyl-2-hydroxymethyl-1H-imidazo[4,5-c]quinoline hydrochloride hydrate. Analysis: Calculated for C13H13N3O.HCl.H2O: %C, 55.4; %H, 5.7; %N, 14.9; Found: %C, 55.2; %H, 5.6; %N, 15.5.

Aufarbeitung

  1. temperaturewas heated at its
  2. temperaturereflux temperature for two hours
  3. temperatureThe solution was cooled
  4. customThe precipitate was separated by filtration
  5. washwashed with water
  6. dissolutionThe solid was redissolved in dilute hydrochloric acid
  7. customreprecipitated with ammonium hydroxide

Quellen und Nachweise

ORD-Eintrag
ord-46bebac8d1f444df907b4bba0fffa8ca
Quelldatensatz
uspto-grants-1987_10
DOI
10.6084/m9.figshare.5104873.v1
Patentnummer
US04698348

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