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Hydrochloric Acid → 4-Phenyl-1,4,5,6-tetrahydropyrimidin-2-amine hydrochloride

HRID 418033
Notizen
Druckvorschau

Reaktionsgleichung

Reaktionsgleichung von HRID 418033
[NH2:1][C:2]1[N:7]=[C:6]([C:8]2[CH:13]=[CH:12][CH:11]=[CH:10][CH:9]=2)[CH:5]=[CH:4][N:3]=1.[ClH:14]>C(O)(C)C.[Pd]>[ClH:14].[C:8]1([CH:6]2[NH:7][C:2]([NH2:1])=[N:3][CH2:4][CH2:5]2)[CH:9]=[CH:10][CH:11]=[CH:12][CH:13]=1
KomponentenVersuchsvorschriftAufarbeitungQuellen und NachweiseNotizen zur Reaktion

Komponenten

5

Edukt 2

HCID 313Hydrochloric AcidHCID 5987772-Amino-4-phenylpyrimidine

Produkt 1

HCID 230261524-Phenyl-1,4,5,6-tetrahydropyrimidin-2-amine hydrochlorideAusbeute 55 %

Reagenzien, Katalysatoren, Lösungsmittel 2

HCID 23938PalladiumKatalysatorHCID 3776IsopropanolLösungsmittel

Versuchsvorschrift

To a solution of 5 g (29.2 mmoles) of 2-amino-4-phenylpyrimidine in 30 ml of a 6N solution of hydrochloric acid in isopropanol was added 0.1 g of palladium on carbon catalyst (10% wt/wt). The suspension was hydrogenated under 40 psi pressure at room temperature during 3 h. The catalyst was removed by filtration and the solvent evaporated under reduced pressure. Diethyl ether was added and the resulting solution was refiltered and the solvent removed by evaporation under reduced pressure to give 4.0 g (55%) of compound as a crude oil which was used as such.

Aufarbeitung

  1. customThe catalyst was removed by filtration
  2. customthe solvent evaporated under reduced pressure
  3. additionDiethyl ether was added
  4. customthe solvent removed by evaporation under reduced pressure

Quellen und Nachweise

ORD-Eintrag
ord-6c4f139a080b4d238635ece9d964c1e9
Quelldatensatz
uspto-grants-2012_01
DOI
10.6084/m9.figshare.5104873.v1
Patentnummer
US08093256B2

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