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Hydrochloric Acid → 3-(5-Amino-1-methylpyrazol-4-yl)propylamine dihydrochloride

HRID 349523
Notizen
Druckvorschau

Reaktionsgleichung

Reaktionsgleichung von HRID 349523
[NH2:1][C:2]1[N:6]([CH3:7])[N:5]=[CH:4][C:3]=1[CH2:8][CH2:9][CH2:10][N:11]1C(=O)C2=CC=CC=C2C1=O.[ClH:22]>O>[ClH:22].[ClH:22].[NH2:1][C:2]1[N:6]([CH3:7])[N:5]=[CH:4][C:3]=1[CH2:8][CH2:9][CH2:10][NH2:11]
KomponentenVersuchsvorschriftAufarbeitungQuellen und NachweiseNotizen zur Reaktion

Komponenten

4

Edukt 2

HCID 313Hydrochloric AcidHCID 179620255-Amino-1-methyl-4-(3-phthalimidopropyl)pyrazole

Produkt 1

HCID 179620333-(5-Amino-1-methylpyrazol-4-yl)propylamine dihydrochloride

Reagenzien, Katalysatoren, Lösungsmittel 1

HCID 962WaterLösungsmittel

Versuchsvorschrift

5-Amino-1-methyl-4-(3-phthalimidopropyl)pyrazole (1.42 g, 5 mmol) was added to concentrated hydrochloric acid (10 ml) at room temperature, and the mixture was stirred under reflux for 23 hours. To the reaction mixture was added water (50 ml), and most of insoluble materials were removed by filtration. The filtrate was washed with ethyl acetate, and the aqueous layer was concentrated in vacuo. The residue was triturated with 2-propanol and dried in vacuo to give 3-(5-amino-1-methylpyrazol-4-yl)propylamine dihydrochloride (700 mg) as a solid.

Aufarbeitung

  1. temperatureunder reflux for 23 hours
  2. custommost of insoluble materials were removed by filtration
  3. washThe filtrate was washed with ethyl acetate
  4. concentrationthe aqueous layer was concentrated in vacuo
  5. customThe residue was triturated with 2-propanol
  6. customdried in vacuo

Quellen und Nachweise

ORD-Eintrag
ord-106e3c25fe28488ab8f6102497abc411
Quelldatensatz
uspto-grants-2007_02
DOI
10.6084/m9.figshare.5104873.v1
Patentnummer
US07179801B2

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