Fused quinoline derivative and use thereof

Organic compounds -- part of the class 532-570 series – Organic compounds – Heterocyclic carbon compounds containing a hetero ring...

Reexamination Certificate

Rate now

  [ 0.00 ] – not rated yet Voters 0   Comments 0

Details

C514S290000

Reexamination Certificate

active

07973163

ABSTRACT:
The present invention aims at provision of a quinoline derivative having a neurokinin 2 (NK2) receptor antagonistic action and relates to a compound represented by the formula (I)wherein R1is a hydrogen atom and the like; R2is a hydrogen atom, a hydrocarbon group optionally having substituent(s) and the like; R3is unsubstituted (i.e., absence), a hydrogen atom and the like; R4and R5are the same or different and each is a hydrogen atom, a hydrocarbon group optionally having substituent(s), and the like; R6is (cyclic group optionally having substituent(s))-carbonyl, and the like; R7, R8, R9and R10are the same or different and each is a hydrogen atom, halogen and the like; or R7and R8, R8and R9, and R9and R10may form a ring together with the adjacent carbon atoms; n is an integer of 1 to 5;--- represents unsubstituted (i.e., absence) or a single bond; andrepresents a single bond or a double bond, or a salt thereof, and the like.

REFERENCES:
patent: 5288725 (1994-02-01), Witherup et al.
patent: WO-94/09001 (1994-04-01), None
patent: WO-02/38547 (2002-05-01), None
patent: WO-02/38548 (2002-05-01), None
patent: WO-02/083663 (2002-10-01), None
patent: WO-02/083664 (2002-10-01), None
Journal of Organic Chemistry, vol. 65, pp. 655-666 (2000).
Journal of Medicinal Chemistry, vol. 35, pp. 1845-1852 (1992).
K. Frank et al., “Cyclizations of Substituted Benzylidene-3-alkenylamines: Synthesis of the Tricyclic Core of the Martinellines,”J. Org. Chem., vol. 65, pp. 655-666 (2000).
C. Leach et al., “Reversible Inhibitors of the Gastric (H+/K+)-ATPase. 2: 1-Arylpyrrolo[3,2-c]quinolines: Effect of the 4-Substituent,”J. Med. Chem., vol. 35, pp. 1845-1852 (1992).
D. Ma et al., “Aromatic Nucleophilic Substitution or Cul-Catalyzed Coupling Route to Martinellic Acid,”J. Org. Chem., vol. 68, pp. 442-451 (2003).
D. Ma et al., “First Total Synthesis of Martinellic Acid, a Naturally Occurring Bradykinin Receptor Antagonist,”Organic Letters, vol. 3, pp. 2189-2191 (2001).
M. Hadden et al., “Synthesis and reactivity of hexahydropyrroloquinolines,”Tetrahedron, vol. 57, pp. 5615-5624 (2001).
M. Hadden et al, “Regioselective Synthesis of Pyrroloquinolines—Approaches to Martinelline,”Tetrahedron Letters, vol. 40, pp. 1215-1218 (1999).
B. Snider et al., Synthesis of the Tricyclic Triamine Core of Martinelline and Martinellic Acid,Tetrahedron Letters, vol. 40, pp. 3339-3342 (1999).
M. Nyerges, “Construction of Pyrrolo[3,2-c]quinolines—Recent Advances in the Synthesis of the Martinelline Alkaloids,”Heterocycles, vol. 63 pp. 1685-1712 (2004).
B. Snider et al., “Total Synthesis of (±)—Martinellic Acid,” Organic Letters, vol. 3, pp. 4217-4220 (2001).

LandOfFree

Say what you really think

Search LandOfFree.com for the USA inventors and patents. Rate them and share your experience with other people.

Rating

Fused quinoline derivative and use thereof does not yet have a rating. At this time, there are no reviews or comments for this patent.

If you have personal experience with Fused quinoline derivative and use thereof, we encourage you to share that experience with our LandOfFree.com community. Your opinion is very important and Fused quinoline derivative and use thereof will most certainly appreciate the feedback.

Rate now

     

Profile ID: LFUS-PAI-O-2667393

  Search
All data on this website is collected from public sources. Our data reflects the most accurate information available at the time of publication.