Substituted N-methyl-N-(4-(piperidin-1-yl)-2-(aryl)butyl)benzami

Drug – bio-affecting and body treating compositions – Designated organic active ingredient containing – Having -c- – wherein x is chalcogen – bonded directly to...

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514321, 514322, 514327, 546194, 546199, 546198, 546221, C07D40106, A61K 31445

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active

059984392

ABSTRACT:
The present invention relates to novel substituted N-methyl-N-(4-(piperidin-1-yl)-2-(aryl)butyl)benzamide derivatives of the formula ##STR1## stereoisomers thereof, and pharmaceutically acceptable salts thereof which are useful as histamine receptor antagonists and tachykinin receptor antagonists. Such antagonists are useful in the treatment of allergic rhinitis, including seasonal rhinitis and sinusitis; inflammatory bowel diseases, including Crohn's disease and ulcerative colitis; asthma; bronchitis; and emesis.

REFERENCES:
patent: 3282947 (1966-11-01), Grogan
patent: 3862173 (1975-01-01), Carr
patent: 4254129 (1981-03-01), Carr
patent: 4254130 (1981-03-01), Carr
patent: 4285958 (1981-08-01), Carr
patent: 4550116 (1985-10-01), Soto
patent: 4598079 (1986-07-01), Beyerle
patent: 4666905 (1987-05-01), Downs
patent: 4835161 (1989-05-01), Janssens
patent: 4908372 (1990-03-01), Carr
patent: 4960776 (1990-10-01), Walsh
patent: 4988689 (1991-01-01), Janssens
patent: 5023256 (1991-06-01), Roberto
patent: 5064850 (1991-11-01), Carr
patent: 5166136 (1992-11-01), Ward
patent: 5182399 (1993-01-01), Kane
patent: 5212187 (1993-05-01), Alisch
patent: 5214040 (1993-05-01), Cuberes-Altisent
patent: 5236921 (1993-08-01), Emonds-Alt
patent: 5272150 (1993-12-01), Janssens
patent: 5317020 (1994-05-01), Emonds-Alt
patent: 5322850 (1994-06-01), Orjales-Venero
patent: 5350852 (1994-09-01), Sanofi
patent: 5371093 (1994-12-01), Carr
patent: 5411971 (1995-05-01), Sanofi
patent: 5434158 (1995-07-01), Shah
patent: 5534525 (1996-07-01), Miller
Barnes, et al., TIPS 11:185-189 (May 1990).
Ichinose, et al., The Lancet 340:1248-1251 (Nov. 21, 1992).
Hagiwara, et al., "Studies on Neurokinin Antagonists 2.", Journal of Medicinal Chemistry, vol. 35, No. 17, 3184-3191, 1992.
Hagiwara, et al., Studies on Neurokinin Antagonists 1., J. Med. Chem, 35, 2015-2025, 1992.
Janssens, et al., J. Med. Chem. 28:1934-1943, (1985).
Janssens, et al., Drug Development Research 8:27-36, (1986).
Jannssens, et al., J. Med. Chem., 28 (12): 1925-1933, (1985).
Iemura, et al., Chem. Pharm. Bull., 37(4):967-972, (1989).
Janssens, et al., J. Med. Chem., 28(12):1943-1947, (1985).
Carr et al., The J. Organic Chem., 55(4): 1399-1401, (1990).
Iemura, et al., Chem. Pharm. Buul., 37(4):962-966, (1989).
Maynard, Biorganic and Medicinal Chemistry Letters, vol. 3 (4), 753-756, 1993).
Wahlgren, J. Heterocyclic Chem., 26, 541-543, 1989.
Iemura, Chem. Pharm. Bull., 37(4), 967-972, 1989.
Iemura, J. Heterocyclic Che., 24, 31-37, 1987.
Iemura, et al., J. Med. Chem., 29(7):1178-1183, (1986).
Hagiwara, et al., Studies on Neurokinin Antagonists 3., J. Med. Chem, 36, 2266-2278, 1993.
Emonds-Alt, et al., Life Sciences, 56(1):27-32, (1995).
Melloni, et al., Eur. J. Med. Chem., 26, 207-213 (1991).
Armour, et al, Biorganic & Med. Chem Ltrs, 6(9), 1015,1020 (1996).
Ward, et al, J. Med. Chem., 38, 4985-4992 (1995).

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