Triethylamine → N-2-(4-(2-Pyrimidinyl)-1-piperazinyl)ethyl-1-methylcyclohexylcarboxamide
Reaktionsgleichung
[N:1]1[CH:6]=[CH:5][CH:4]=[N:3][C:2]=1[N:7]1[CH2:12][CH2:11][N:10]([CH2:13][CH2:14][NH2:15])[CH2:9][CH2:8]1.[CH3:16][C:17]1([C:23](Cl)=[O:24])[CH2:22][CH2:21][CH2:20][CH2:19][CH2:18]1.C(N(CC)CC)C>>[N:1]1[CH:6]=[CH:5][CH:4]=[N:3][C:2]=1[N:7]1[CH2:12][CH2:11][N:10]([CH2:13][CH2:14][NH:15][C:23]([C:17]2([CH3:16])[CH2:22][CH2:21][CH2:20][CH2:19][CH2:18]2)=[O:24])[CH2:9][CH2:8]1Komponenten
4
Versuchsvorschrift
The title compound was prepared from 2-(4-(2-pyrimidinyl)-1-piperazinyl)ethyl amine (1.50 g, 0.00724 mol), 1-methylcyclohexylcarboxylic acid chloride (1.16 g, 0.00722 mol) and triethylamine (1.1 mL, 0.80 g, 0.0079 mol) in the manner previously described to give 1.80 g (62%) of product, mp. 212°-220° C.
Quellen und Nachweise
- ORD-Eintrag
- ord-343061f1fa8348f9a1170f0e302ca1ff
- Quelldatensatz
- uspto-grants-1991_01
- Patentnummer
- US04988814
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