M-Cresol → HCID 178511983, Verbindung
Reaktionsgleichung
Cl.Cl.[NH2:3][C:4]1[CH:16]=[CH:15][CH:14]=[CH:13][C:5]=1[CH2:6][N:7]1[CH2:12][CH2:11][O:10][CH2:9][CH2:8]1.[C:17]([N:19]1[CH2:24][CH2:23][O:22][CH2:21][CH2:20]1)#[N:18].C1C(O)=CC=CC=1C>>[O:10]1[CH2:9][CH2:8][N:7]([CH2:6][C:5]2[CH:13]=[CH:14][CH:15]=[CH:16][C:4]=2[NH:3][C:17]([N:19]2[CH2:24][CH2:23][O:22][CH2:21][CH2:20]2)=[NH:18])[CH2:12][CH2:11]1Komponenten
4
Versuchsvorschrift
A mixture of 4(2-aminobenzyl)morpholine dihydrochloride (6.8 g), 4-cyanomorpholine (4.3 g) and m-cresol was heated at 90°-95° C. for 12 hours to yield N-(2-morpholinomethylphenyl)morpholine-4-carboxamidine (m.p. 118°-119° C.) which was recrystallised from hexane and then converted into its difumarate salt (m.p. 166°-167° C.) which was recrystallised from propan-2-ol.
Aufarbeitung
- temperaturewas heated at 90°-95° C. for 12 hours
Quellen und Nachweise
- ORD-Eintrag
- ord-14642c1a813541fb9ce1ef03e2020228
- Quelldatensatz
- uspto-grants-1993_06
- Patentnummer
- US05223498
Notizen zur Reaktion
Wird geladen…