Cyanoquinoline compounds

US5565408A · kind A · utility

Assignee

• BASF SE

Inventors

• Helmut Hagen · Bischofswerda, DE
• Juergen Pfister · Speyer, DE
• Gunter Brill · Haßloch, DE
• Gerhard Nilz · Schifferstadt, DE
• Bruno Wuerzer · Otterstadt, DE
• Karl-Otto Westphalen · Speyer, DE

Key dates

• Filing date: Apr 17, 1995
• Grant date: Oct 15, 1996
• Expiry date: Apr 17, 2015

Classification

• Technology area (CPC C): Chemistry; Metallurgy
• CPC primary: C07D401/12
• WIPO field: Organic fine chemistry
• WIPO sector: Chemistry

Abstract

Cyanoquinoline compounds Ia or Ib ##STR1## where R.sup.1 is CH.dbd.C(CN).sub.2 ; CH.dbd.N--N.dbd.CH--(5-quinolyl); methylsulfonyl; CH.dbd.NOH; halogen; hydroxyl; nitro; cyano; unsubstituted or substituted C.sub.1 -C.sub.4 -alkyl, C.sub.1 -C.sub.4 -alkoxy or C.sub.1 -C.sub.4 -alkylthio, pyrrolidinyl; piperidinyl; morpholinyl; thiomorpholinyl; unsubstituted or substituted phenyl, phenoxy, phenylthio, phenyldithiolyl, phenylsulfonyl or pyrrolyl; PA1 m is 0, 1, 2 or 3; PA1 R.sup.2 is hydrogen; hydroxyl; halogen; C.sub.1 -C.sub.4 -alkoxy; --NR.sup.3 R.sup.4 ; --NR.sup.5 --CXR.sup.6 or --N.dbd.CR.sup.7 R.sup.8 ; PA1 R.sup.3 is hydrogen or unsubstituted or substituted C.sub.1 -C.sub.4 -alkyl; PA1 R.sup.4 is a radical R.sup.3 ; C.sub.1 -C.sub.4 -alkylamino; di-C.sub.1 -C.sub.4 -alkylamino; substituted C.sub.1 -C.sub.4 -alkyl; CH.dbd.N--(3-cyano-2-quinolinyl); or R.sup.3 and R.sup.4 together form C.sub.4 - or C.sub.3 -alkylene which may be interrupted by a hetero atom, or unsubstituted or substituted 1,3-butadienyl; PA1 R.sup.5 and R.sup.7 are each hydrogen or C.sub.1 -C.sub.4 -alkyl; PA1 R.sup.6 and R.sup.8 are each a radical R.sup.5 ; substituted C.sub.1 -C.sub.4 -alkyl; C.sub.3 -C.sub.7 …