N-Methyl-1,3-propanediamine → HCID 178480416, Verbindung
Reaktionsgleichung
I.CS[C:4](=[NH:18])[NH:5][C:6]1[CH:11]=[CH:10][CH:9]=[CH:8][C:7]=1[N:12]1[CH2:17][CH2:16][O:15][CH2:14][CH2:13]1.[CH3:19][NH:20][CH2:21][CH2:22][CH2:23]N>C(O)C>[CH3:19][N:20]1[CH2:21][CH2:22][CH2:23][NH:18][C:4]1=[N:5][C:6]1[CH:11]=[CH:10][CH:9]=[CH:8][C:7]=1[N:12]1[CH2:17][CH2:16][O:15][CH2:14][CH2:13]1Komponenten
4
Edukt 2
Produkt 1
Reagenzien, Katalysatoren, Lösungsmittel 1
Versuchsvorschrift
A mixture of 2-methyl-1-(2-morpholinophenyl)-2-thiopseudourea hydroiodide (3.8 g prepared as described in Example 166), 3-methylaminopropylamine (2.6 g) and absolute ethanol (40 ml) was heated under reflux for 6 hours to give a solid which was recrystallised from ether to give 4-[2-(1-methylperhydropyrimidin-2-ylideneamino)phenyl]morpholine (m.p. 138°-139° C.).
Aufarbeitung
- temperaturewas heated
- temperatureunder reflux for 6 hours
- customto give a solid which
- customwas recrystallised from ether
Quellen und Nachweise
- ORD-Eintrag
- ord-a88b0f5037bb42ecb765699a00bdde64
- Quelldatensatz
- uspto-grants-1994_12
- Patentnummer
- US05373008
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