2,4-Dichlorobenzylidenemalononitrile → 5-Aminomethyl-6-(2,4-dichloro-phenyl)-2-morpholin-4-yl-pyrimidin-4-ylamine

HRID 1793911

Reaktionsgleichung

[N:1]1([C:7]([NH2:9])=[NH:8])[CH2:6][CH2:5][O:4][CH2:3][CH2:2]1.[Cl:10][C:11]1[CH:22]=[C:21]([Cl:23])[CH:20]=[CH:19][C:12]=1[CH:13]=[C:14]([C:17]#[N:18])[C:15]#[N:16]>>[NH2:18][CH2:17][C:14]1[C:15]([NH2:16])=[N:8][C:7]([N:1]2[CH2:6][CH2:5][O:4][CH2:3][CH2:2]2)=[N:9][C:13]=1[C:12]1[CH:19]=[CH:20][C:21]([Cl:23])=[CH:22][C:11]=1[Cl:10]

Komponenten

Edukt 2

HCID 180892,4-Dichlorobenzylidenemalononitrile

HCID 205053Morpholinoamidine

Produkt 1

HCID 103089935-Aminomethyl-6-(2,4-dichloro-phenyl)-2-morpholin-4-yl-pyrimidin-4-ylamine

Versuchsvorschrift

The title compound, MS: m/e=353.9 (M+), was prepared from morpholine-4-carboxamidine and 2-(2,4-dichloro-benzylidene)-malononitrile in analogy to the process described in Example 11 as a solid.

Quellen und Nachweise

ORD-Eintrag: ord-00faaf90d3fe4aba9bc8135b4a2b9c8e
Quelldatensatz: uspto-grants-2006_04
DOI: 10.6084/m9.figshare.5104873.v1
Patentnummer: US07022718B2

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