6'-(1-Adamantanecarboxylate)-6-O-α-D-galactopyranosyl-α-D-glucopyranose sulfate salts

Claim 2

A compound selected from those of the formula: ##STR5## wherein A is a pharmaceutically acceptable cation salt, wherein the salt forming moiety is selected from the group consisting of alkali metal, alkaline earth metal, ammonia and substituted ammonia selected from the group consisting of trialkylamine (C 1 -C 6 ), piperidine, pyrazine, alkanolamine (C 2 -C 6 ) and cycloalkylamine (C 3 -C 6 ).

Claim 3

The compound according to claim 1, 6'-(1-adamantanecarboxylate)-6-O-α-D-galactopyranosyl-α-D-glucopyranose, heptakis (H-sulfate), heptasalt with trimethylamine.

Claim 4

The compound according to claim 1, 6'-(1-adamantanecarboxylate)-6-O-α-D-galactopyranosyl-α-D-glucopyranose, heptakis (H-sulfate), heptasodium salt.

Claim 9

The method according to claim 4 or 5, wherein the compound is 6'-(1-adamantanecarboxylate)-6-O-α-D-galactopyranosyl-α-D-glucopyranose, heptakis (H-sulfate), heptasalt with trimethylamine.

Claim 10

The method according to claim 4 or 5, wherein the compound is 6'-(1-adamantanecarboxylate)-6-O-α-D-galactopyranosyl-α-D-glucopyranose, heptakis (H-sulfate), heptasodium salt.

Claim 11

The method according to claim 5, wherein the compound is administered internally.

Claim 12

The method according to claim 5, wherein the compound is administered topically.

Claim 13

The method according to claim 5, wherein the compound is administered periodontally in the oral cavity.

Claim 14

The method according to claim 5, wherein the compound is administered intra-articularly.

Claim 15

The method according to claim 5, wherein the compound is administered parenterally.

Claim 16

A process for the preparation of a compound of the formula: ##STR8## wherein A is a pharmaceutically acceptable cation salt, wherein the salt forming moiety is selected from the group consisting of alkali metal, alkaline earth metal, ammonia and substituted ammonia selected from the group consisting of trialkylamine (C 1 -C 6 ), piperidine, pyrazine, alkanolamine (C 2 -C 6 ) and cycloalkylamine (C 3 -C 6 ), which comprises suspending 6-O-α-D-galactopyranosyl-α-D-glucopyranose in pyridine, adding calcium sulfate, heating at 75°-100° C. for 15-60 minutes, adding trityl chloride, heating and stirring for 2 hours, cooling, adding acetic anhydride, standing overnight, collecting solid 6-O-(6-O-trityl-α-D-galactopyranosyl)-α-D-glucopyranose, heptaacetate, heating with glacial acetic acid at 40°-70° C. for 4 hours, cooling and extracting with dichloromethane, evaporating extracts to a glass and purifying giving 6-O-α-D-galactopyranosyl-α-D-glucopyranose, heptaacetate, treating with 1-adamantoylchloride in pyridine with stirring for 20 hours, pouring into ice, giving 6'-(1-adamantanecarboxylate)-6-O-α-D-galactopyranosyl-α-D-glucopyranose, heptaacetate, dissolving in methanol:water:triethylamine (6:2:3), stirring for 24 hours and evaporating, giving 6'-(1-adamantanecarboxylate)-6-O-α-D-galactopyranosyl-α-D-glucopyranose, adding to a mixture of trimethylamine-sulfur trioxide in dimethylformamide and stirring for 24 hours, giving 6'-(1-adamantanecarboxylate)-6-O-α-D-galactopyranosyl-α-D-glucopyranose, heptakis (H-sulfate), heptasalt with trimethylamine and treating with an alkali metal or alkaline earth metal cation-containing compound or ammonia or a substituted ammonia other than trimethylamine selected from the group consisting of trialkylamine (C 1 -C 6 ), piperidine, pyrazine, alkanolamine (C 2 -C 6 ) and cycloalkylamine (C 3 -C 6 ).

Claim 17

A process for the preparation of a compound of the formula: ##STR8## wherein A is a pharmaceutically acceptable cation salt, wherein the salt forming moiety is selected from the group consisting of alkali metal, alkaline earth metal, ammonia and substituted ammonia selected from the group consisting of trialkylamine (C 1 -C 6 ), piperidine, pyrazine, alkanolamine (C 2 -C 6 ) and cycloalkylamine (C 3 -C 6 ), which comprises suspending 6-O-α-D-galactopyranosyl-α-D-glucopyranose in pyridine, adding calcium sulfate, heating at 75°-100° C. for 15-60 minutes, adding trityl chloride, heating and stirring for 2 hours, cooling, adding acetic anhydride, standing overnight, collecting solid 6-O-(6-O-trityl-α-D-galactopyranosyl)-α-D-glucopyranose, heptaacetate, heating with glacial acetic acid at 40°-70° C. for 4 hours, cooling and extracting with dichloromethane, evaporating extracts to a glass and purifying giving 6-O-α-D-galactopyranosyl-α-D-glucopyranose, heptaacetate, treating with 1-adamantoylchloride in pyridine with stirring for 20 hours, pouring into ice, giving 6'-(1-adamantanecarboxylate)-6-O-α-D-galactopyranosyl-α-D-glucopyranose, heptaacetate, dissolving in methanol:water:triethylamine (6:2:3), stirring for 24 hours and evaporating, giving 6'-(1-adamantanecarboxylate)-6-O-α-D-galactopyranosyl-α-D-glucopyranose, adding to a mixture of trimethylamine-sulfur trioxide in dimethylformamide and stirring for 24 hours, giving 6'-(1-adamantanecarboxylate)-6-O-α-D-galactopyranosyl-α-D-glucopyranose, heptakis (H-sulfate), heptasalt with trimethylamine and treating with an alkali metal or alkaline earth metal cation-containing compound or ammonia or a substituted ammonia other than trimethylamine selected from the group consisting of trialkylamine (C 1 -C 6 ), piperidine, pyrazine, alkanolamine (C 2 -C 6 ) and cycloalkylamine (C 3 -C 6 ).