Sanofi

C M Industries

Sergio Boveri

Robert Boigegrain

Roberto Cecchi

Dino Nisato

Paolo Carminati

Romeo Roncucci

Andrea Pedrazzoli

Alberto Bianchetti

A process for the preparation of a compound of formula (I) ##STR1## which is a (RR) and (RS) stereoisomer of N-(7-ethoxycarbonylmethoxy-1,2,3,4,-tetrahydronaphth-2-yl)-2-(3-chlorophen yl)-2-hydroxyethanamine and their pharmaceutically acceptable salts.

(RR) and (RS stereoisomers of

A process for the preparation of phenylethanolaminotetralins of formula ##STR1## wherein X is hydrogen, a halogen, a trifluoromethyl or a lower alkyl group and R.sup.o is hydrogen or a methyl group substituted by a carboxy or a lower carbalkoxy group, which comprises treating a mandelic acid with a 2-amino-7-hydroxytetralin, optionally alkylating with a lower alkyl haloacetate and reducing the amido group of the mandelamide into a methyleneamino group. The mandelamides intermediates are novel.

Process for the preparation of phenylethanolaminotetralins

2-amino-7-hydroxytetraline ethers of formula ##STR1## wherein R' represents methyl substituted by a carboxy group or lower carbalkoxy group or a salt thereof; a process for their preparation starting from the 2-amino-7-hydroxytetraline, N-protection, O-alkylation and N-deprotection; N-protected intermediates; and use of the compounds I for the preparation of the corresponding phenylethanolaminotetralines.

2-amino-7-hydroxytetraline ethers

A process for the preparation of phenylethanolaminotetralins of formula ##STR1## wherein X is hydrogen, a halogen, a trifluoromethyl or a lower alkyl group and R.degree. is hydrogen or a methyl group substituted by a carboxy or a lower carbalkoxy group, which comprises treating a mandelic acid with a 2-amino-7-hydroxytetralin, optionally alkylating with a lower alkyl haloacetate and reducing the amido group of the mandelamide into a methyleneamino group. The mandelamides intermediates are novel.

A process for the preparation of a compound of formula ##STR1## wherein X represents hydrogen, halogen, trifluoromethyl or lower alkyl group; W represents methyl, Q represents hydrogen or W and Q, together, form an ethylene group and R' represents a lower alkyl group which comprises protecting the amino group of the phenol corresponding to the compound of formula I, submitting the compound thus obtained to an alkylation (with a compound of formula Hal--CH.sub.2 --COOR', wherein R' is as defined hereinabove for the formula I and Hal is chlorine, bromine or iodine) and then releasing the amino group of the product thus obtained.

Process for the O-alkylation of N-(hydroxy)aralkylphenylethanolamines

Benzamides having histamine H.sub.2 receptor blocking activity of formula ##STR1## wherein A represents O, S, N--CN or CH--NO.sub.2 and R represents an alkyl group or an optionally substituted phenyl, pyridyl or pyridyl 1-oxide group; their salts; a process for their preparation; and pharmaceutical compositions containing them as active ingredients.

3-Amino-n-[2-(5-dimethylaminomethylfuran-2-ylmethylthio)ethyl]benzamide

N-substituted nicotinamide 1-oxide having histamine H.sub.2 receptor blocking activity of formula ##STR1## wherein X is a nitrogen atom or a CH group and Am represents a mono- or disubstituted amino group, a pyrrolidino, morpholino, thiomorpholino, hexamethyleneimino group, or an optionally substituted piperidino or piperazino group; their salts; a process for their preparation; and pharmaceutical compositions containing them as active ingredients.

N-substituted nicotinamide 1-oxide as histamine H.sub.2 receptor blockers

Amides acting as histamine H.sub.2 receptors antagonists, of formula ##STR1## wherein X represents a N.fwdarw.O or C-NH-A-B group in which A is CO or SO.sub.2 and B is alkyl, phenyl, pyridyl, pyridyl 1-oxide, pyrazinyl or thienyl; their salts; process for their preparation by reacting 2-(2-guanidinothiazol-4-ylmethylthio)ethylamine with a derivative of formula ##STR2## and optional salification; and pharmaceutical compositions containing same.

Certain amide derivatives of 2-guanidino-thiazoles and compositions

Benzamides, their salts, and pharmaceutical compositions containing them

The invention relates to thioalkylamide of nicotinic acid 1-oxide with H.sub.2 receptor blocking activity, of formula: ##STR1## and to its pharmaceutically acceptable salts, to a process for preparing same by reaction of 2-(5-dimethylaminomethylfuran-2-ylmethylthio)ethylamine with a functional derivative of nicotinic acid 1-oxide and possible salification, and to pharmaceutical compositions containing same.

Thioalkylamide of nicotinic acid 1-oxide, its salts, and pharmaceutical

Amidobenzamides acting as histamine H.sub.2 receptors blocking agents, of formula ##STR1## wherein A is CO or SO.sub.2 and B is alkyl, phenyl, pyridyl, pyridyl-1-oxyde, pyrazinyl or thienyl; their salts; process for their preparation by reaching 2-(5-dimethyl-aminomethylfuran-2-ylmethylthio)ethylamine with a derivative of formula ##STR2## and optional salification and pharmaceutical compositions containing same.

Amidobenzamides, their salts and pharmaceutical compositions containing

Talampicillin 2-methoxyphenoxyacetate; a process for its preparation by acid hydrolysis of the metampicillin phthalidyl ester in a biphasic aqueous-organic solvent and treatment of the resulting aqueous phase with an alkali metal salt of the 2-methoxyphenoxyacetic acid; and pharmaceutical compositions containing said talampicillin 2-methoxyphenoxyacetate as an active ingredient.

Talampicillin 2-methoxyphenoxyacetate and pharmaceutical compositions

Anti-anaphylactic and anti-allergic 5-(2-hydroxy-3-thiopropoxy) chromone-2-carboxylic acids of the general formula ##STR1## wherein R is alkyl, alkenyl, hydroxyalkyl, cycloalkyl, cyclo-alkylalkyl, their alkali and alkaline-earth metal salts and 1-4 C alkyl esters as well as a process for the preparation thereof and pharmaceutical compositions containing them.

Growing community of inventors

Tortona, Italy

Sergio Boveri