Reaktionsgleichung
[CH:1]1[C:10]2[CH:9]=[CH:8][CH:7]=[C:6]([S:11]([N:14]3[CH2:20][CH2:19][CH2:18][NH:17][CH2:16][CH2:15]3)(=[O:13])=[O:12])[C:5]=2[CH:4]=[CH:3][N:2]=1.[ClH:21]>CO>[ClH:21].[CH:1]1[C:10]2[CH:9]=[CH:8][CH:7]=[C:6]([S:11]([N:14]3[CH2:20][CH2:19][CH2:18][NH:17][CH2:16][CH2:15]3)(=[O:12])=[O:13])[C:5]=2[CH:4]=[CH:3][N:2]=1Komponenten
4
Reagenzien, Katalysatoren, Lösungsmittel 1
Versuchsvorschrift
5 g of 1-(5-isoquinolinesulfonyl)homopiperazine (Compound(1)) as prepared in substantially the same manner as in Example 3 was dissolved in 40 ml of methanol, and the pH of the solution was adjusted to 6 with 1N hydrochloric acid. Then the solution was condensed under reduced pressure to obtain a crystalline residue. The crystalline residue thus obtained was recrystallized from methanol-ether to obtain 1-(5isoquinolinesulfonyl)homopiperazine hydrochloride. Analytical data on this compound are given below.
Aufarbeitung
- customcondensed under reduced pressure
- customto obtain a crystalline residue
- customThe crystalline residue thus obtained
- customwas recrystallized from methanol-ether
Quellen und Nachweise
- ORD-Eintrag
- ord-c475e692aaaf4926b344fed11d73eb97
- Quelldatensatz
- uspto-grants-1987_07
- Patentnummer
- US04678783
Verknüpfte Notizen
Wird geladen…