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Hydrochloric Acid → 4-isopropyl-4,5,6,7-tetrahydro-1H-imidazo[4,5-c]pyridine hydrochloride

HRID 2383254
Notizen
Druckvorschau

Reaktionsgleichung

Reaktionsgleichung von HRID 2383254
[ClH:1].Cl.[NH2:3][CH2:4][CH2:5][C:6]1[N:10]=[CH:9][NH:8][CH:7]=1.[OH-].[Na+].[CH:13](=O)[CH:14]([CH3:16])[CH3:15].Cl>O.CO>[ClH:1].[CH:14]([CH:16]1[C:7]2[N:8]=[CH:9][NH:10][C:6]=2[CH2:5][CH2:4][NH:3]1)([CH3:15])[CH3:13]
KomponentenReaktionsbedingungenVersuchsvorschriftAufarbeitungQuellen und NachweiseNotizen zur Reaktion

Komponenten

7

Edukt 4

HCID 313Hydrochloric AcidHCID 6561IsobutyraldehydeHCID 14798Sodium HydroxideHCID 178478691HCID 178478691, Verbindung

Produkt 1

HCID 672350744-isopropyl-4,5,6,7-tetrahydro-1H-imidazo[4,5-c]pyridine hydrochlorideAusbeute 48,7 %

Reagenzien, Katalysatoren, Lösungsmittel 2

HCID 887
Methanol
Lösungsmittel
HCID 962WaterLösungsmittel

Reaktionsbedingungen

Temperatur
80 °C

Versuchsvorschrift

Histamine dihydrochloride (61.9 g, 336 mmol) was dissolved in a solution of NaOH (33.6 g, 841 mmol) in water (125 mL) and MeOH (500 mL), and isobutyraldehyde (61.4 mL, 672 mmol) was added. The reaction mixture was heated under reflux at 80° C. for 24 h, cooled to room temperature, the pH was adjusted to 7 with 1 M aq HCl solution (250 mL) and the solvents were removed in vacuo. The residue was dissolved in warm MeOH (300 mL), allowed to stand for 1 h, filtered and the solvents were removed in vacuo. The residue was stirred in MeOH (50 mL) and acetone (400 mL) for 2 h and was cooled to 4° C. for 2 h. The resulting precipitate was filtered and washed with acetone (100 mL) to give 4-isopropyl-4,5,6,7-tetrahydro-1H-imidazo[4,5-c]pyridine hydrochloride (33.0 g, 48.7%) as a white solid.

Aufarbeitung

  1. additionwas added
  2. temperatureThe reaction mixture was heated
  3. temperaturecooled to room temperature
  4. customthe solvents were removed in vacuo
  5. dissolutionThe residue was dissolved in warm MeOH (300 mL)
  6. filtrationfiltered
  7. customthe solvents were removed in vacuo
  8. waitacetone (400 mL) for 2 h
  9. temperaturewas cooled to 4° C. for 2 h
  10. filtrationThe resulting precipitate was filtered
  11. washwashed with acetone (100 mL)

Quellen und Nachweise

ORD-Eintrag
ord-fa44b9505c14461dab0df671fa319f96
Quelldatensatz
uspto-grants-2012_09
DOI
10.6084/m9.figshare.5104873.v1
Patentnummer
US08263616B2

Notizen zur Reaktion

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