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HRID 651348Erstellt: 24. Oktober 2026

Diisopropylethylamine → N-(5-(8-Naphthalen-1-ylmethyl-4-oxo-1-phenyl-1,3,8,-triazaspiro[-4.5]dec-3-yl)pentyl)guanidine

https://huagongshe.com/de/reaction/651348

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktDiisopropylethylamineHCID 81531—
Edukt3,5-Dimethyl-1H-pyrazole-1-carboxamidine mononitrateHCID 198186—
Edukt3-(5-Aminopentyl)-8-naphthalen-1-ylmethyl-1-phenyl-1,3,8-triaza-spiro[4.5]decan-4-oneHCID 20679434—
LösungsmittelWaterHCID 962—
LösungsmittelDimethylformamideHCID 6228—
ProduktN-(5-(8-Naphthalen-1-ylmethyl-4-oxo-1-phenyl-1,3,8,-triazaspiro[-4.5]dec-3-yl)pentyl)guanidineHCID 1785128255,2%

Reaktionsschritte

3-(5-Aminopentyl)-8-naphthalen-1-ylmethyl-1-phenyl-1,3,8-triaza-spiro[4.5]decan-4-one, di-trifluoroacetate (0.137 g, 0.2 mmol) prepared as described in Example 13, was dissolved in dimethylformamide (1 ml) and diisopropylethylamine (0.233 g, 1.8 mmol) and 3,5-dimethylpyrazol-1-carboxamidine nitrate (0.060 g, 0.3 mmol) was added. The mixture was stirred at room temperature for 1 h and the addition of an equal amount 3,5-dimethylpyrazol-1 carboxamidine nitrate was repeated. After stirring for 16 h the mixture was diluted with water (10 ml) and extracted with ether (5×10 ml). The aqueous phase and undissolved syrup were extracted with dichloromethane (10 ml), the dichloromethane solution was washed with water (5×10 ml), dried over MgSO4 and concentrated in vacuo, affording the title compound (0.047 g, 5.2%) as an amorphous powder.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS06277991B1
Quelldatensatzuspto-grants-2001_08
ORD IDord-8e43e02b6f0b472cbbea7341b6042c53
Quellennotizuspto-grants-2001_08