Claims
- 1. A compound of formula (I): ##STR15## in which: A represents ##STR16## R represents linear or branched lower alkyl, RO and A being substituted on different rings,
- R.sub.1 represents hydrogen or linear or branched lower alkyl, and
- R.sub.2 represents aryl or lower aralkyl or aryl or lower arylalkyl substituted by one or more radicals selected from the group consisting of lower alkyl, lower alkoxy, trifluoromethyl and halogen and where aryl means phenyl or naphthyl, or the optical isomers, epimers or diastereoisomers thereof and addition salts thereof with a pharmaceutically-acceptable acid, and that the terms lower alkyl and lower alkoxy as used herein mean such a group having 1 to 6 carbon atoms inclusive.
- 2. A compound as claimed in claim 1, in which the OR group is in position 7, or diastereoisomers thereof or addition salts thereof with a pharmaceutically-acceptable acid.
- 3. a compound as claimed in claim 1, in which R.sub.2 represents:
- aryl or lower arylalkyl unsubstituted or substituted by one or more chlorine atoms or groups chosen from among lower alkyl, lower alkoxy, and trifluoromethyl, or diastereoisomers thereof or addition salts thereof with a pharmaceutically-acceptable acid.
- 4. A compound as claimed in claim 1, in which the OR group is in position 7, R.sub.1 represents hydrogen and R.sub.2 represents aryl or lower arylalkyl unsubstituted or substituted by one or more halogen atoms, or diastereoisomers thereof.
- 5. A compound as claimed in claim 1, which is N-[2-(7-methoxynaphth-1-yl) ethyl]benzamide.
- 6. A compound as claimed in claim 1, which is N-[2-(7-methoxynaphth-1-yl) ethyl]3,5-dichlorobenzamide.
- 7. A pharmaceutical composition useful for treating melatoninergic disorders containing as active ingredient an effective amount of at least one compound as claimed in claim 1 in combination with a pharmaceutically-acceptable inert exciipient or vehicle.
- 8. A method for treating a living animal afflicted with a treatable disorder of the melatoninergic system comprising the step of administering to the said living animal an amount of a compound of claim 1 which is effective for alleviation of the said condition.
Priority Claims (1)
Number |
Date |
Country |
Kind |
90 02393 |
Feb 1990 |
FRX |
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Parent Case Info
The present application is a division of our prior-filed copending application Ser. No. 07/816,466 filed Jan. 3, 1992, now U.S. Pat. No. 5,225,442, issued Jul. 6, 1993, which is in turn a division of Ser. No. 07/661,425, filed Feb. 26, 1991, now U.S. Pat. No. 5,194,614, issued Mar. 16, 1993.
US Referenced Citations (10)
Foreign Referenced Citations (1)
Number |
Date |
Country |
0113033 |
Oct 1978 |
JPX |
Non-Patent Literature Citations (6)
Entry |
Dey et al., Chemical Abstracts, vol. 34, #5085 7,8 (1940). |
Koelsch et al., Chemical Abstracts, vol. 50, #8564h (1956). |
The Merck Index, Eleventh Edition, p. 912 (1989). |
Isoquinolines, IV. Syntheses of benzisoquinolones and investigation of methods to produce isoquinolines from the naphthalene ring., B. B. Dey and S. Rajagopalan, Archives of Pharmacology, 277, 359-374 (1939). |
Preparation and reduction of 2-methoxy-N-methyl-1-napthalene ethylamine, C. F. Koelsch and Horace E. Hood, II Journal of organic Chemistry, 20, 1282-1287 (1955). |
Araki, Chemical Abstracts, vol. 83 (1975) No. 206,008f. |
Divisions (2)
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Number |
Date |
Country |
Parent |
816466 |
Jan 1992 |
|
Parent |
661425 |
Feb 1991 |
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