Hydrochloric Acid → Piperazine, 1-[4,5-bis(trifluoromethyl)-2-pyridinyl]-
Reaktionsgleichung
Cl[C:2]1[CH:7]=[C:6]([C:8]([F:11])([F:10])[F:9])[C:5]([C:12]([F:15])([F:14])[F:13])=[CH:4][N:3]=1.[NH:16]1[CH2:21][CH2:20][NH:19][CH2:18][CH2:17]1.Cl>>[F:9][C:8]([F:11])([F:10])[C:6]1[C:5]([C:12]([F:15])([F:14])[F:13])=[CH:4][N:3]=[C:2]([N:16]2[CH2:21][CH2:20][NH:19][CH2:18][CH2:17]2)[CH:7]=1Komponenten
4
Versuchsvorschrift
Working as described in Example 1, but starting with 10 g (0.04 mol) of 2-chloro-4,5-bis(trifluoromethyl)pyridine and 10.3 g (0.12 mol) of piperazine, the base having a boiling point B.p. 0.04 of 100-102° C. was obtained, and then, after conversion to the hydrochloride, 7.8 g of the title compound .
Aufarbeitung
- custom0.04 of 100-102° C. was obtained
Quellen und Nachweise
- ORD-Eintrag
- ord-c3cc6e9d34d644c5b43208a2f3d2878d
- Quelldatensatz
- uspto-grants-1990_11
- Patentnummer
- US04971969
Notizen zur Reaktion
Wird geladen…