Preparation of ethers of monosaccharides

Claim 2

In a method of preparing an ethereally substituted monosaccharide comprising the step of reacting 1. a monosaccharide derivative having the general formula A-O-H, wherein O is oxygen, H is hydrogen and A is the residue of a monosaccharide selected from the group consisting of pentoses, hexoses and heptoses which has been derivatized with at least one substance selected from the group consisting of (1-a) at least one alcohol containing 1-18 carbon atoms to produce an acetal group at the site of at least one available hydroxyl residue. (1-b) at least one aldehyde containing 1-18 carbon atoms to produce at least one acetal group at the site of at least one available hydroxyl residue, (1-c) at least one ketone containing 1-18 carbon atoms to produce at least one ketal group at the site of at least one available hydroxyl residue, and (1-d) at least one organic acid residue containing 1-18 carbon atoms to produce an ester group at the site of at least one available hydroxyl residue, the said hydrolyzable acetal groups (1-a) and (1-b), ketal group (1-c) and ester group (1-d) being removable from said A by hydrolysis in an acidic aqueous medium having a pH value less than 7, 2. an organic halide having the general formula Y-X, wherein X is selected from the group consisting of chlorine, bromine and iodine and Y is selected from the group consisting of (2-a) cyclic monovalent nitrogen containing organic radicals and residua free of carbonyl oxygen and (2-b) monovalent organic radicals and residua having the general formula --R 1 --B, wherein B is selected from the group consisting of ##STR5## --O--R 4 and --S--R 4 , R 1 is a divalent organic radical having a linear carbon chain length of about 1-7 carbon atoms, R 2 and R 3 are selected from the group consisting of --H, --OH, --SH, halogen and monovalent organic radicals and residua having a linear carbon chain length of about 1-7 carbon atoms, R 4 is selected from the group consisting of --H and monovalent organic radicals and residua having a linear carbon chain length of about 1-7 carbon atoms, N is nitrogen, O is oxygen, S is sulphur and H is hydrogen, the said hydrogen atom H of the monosaccharide derivative A-O-H and the said halogen atom X of the organic halide being reactive whereby the said H is replaced by Y to produce an ethereally substituted monosaccharide derivative having the general formula A-O-Y wherein A and Y are as above defined, the improvement which comprises reacting said monosaccharide derivative (1) and the said organic halide (2) at an elevated reaction temperature below the thermal decomposition temperature thereof while dissolved in an anhydrous organic solvent in the present of a solid anhydrous strong inorganic base of a metal selected from the group consisting of the alkali metals and the alkaline earth metals and in the presence of a dehydrating agent which is a scavenger for water whereby anhydrous reaction conditions are maintained throughout the reaction.

Claim 3

The method of claim 1 wherein the dehydrating agent is anhydrous calcium chloride.

Claim 4

The method of claim 1 wherein the organic solvent is selected from the group consisting of 1,4-dioxane and tetrahydrofuran.

Claim 5

The method of claim 1 wherein the said inorganic base is selected from the group consisting of the anhydrous oxides and hydroxides of sodium, potassium and calcium.

Claim 6

The method of claim 1 wherein Y is ##STR6## R 1 is a hydrocarbon radical having a linear carbon chain length of 1-3 carbon atoms, and R 2 and R 3 are selected from the group consisting of hydrogen and hydrocarbon radicals having a linear carbon chain length of 1-3 carbon atoms.

Claim 7

The method of claim 1 wherein Y is -(N',N'-dimethylamino-n-propyl).

Claim 8

In a method of preparing an ethereally substituted monosaccharide comprising the steps of reacting 1. a monosaccharide derivative having the general formula A 1 -O-H, wherein O is oxygen, H is hydrogen and A 1 is the residue of a monosaccharide selected from the group consisting of pentoses, hexoses and heptoses which has been derivatized with at least one substance selected from the group consisting of (1-a) at least one alcohol containing 1-18 carbon atoms to produce a hydrolyzable acetal group at the site of at least one available hydroxyl residue, (1-b) at least one aldehyde containing 1-18 carbon atoms to produce at least one hydrolyzable acetal group at the site of at least one available hydroxyl residue, (1-c) at least one ketone containing 1-18 carbon atoms to produce at least one hydrolyzable ketal group at the site of at least one available hydroxyl residue, and (1-d) at least one organic acid residue containing 1-18 carbon atoms to produce a hydrolyzable ester group at the site of at least one available hydroxyl residue, the said hydrolyzable acetal groups (1-a) and (1-b), ketal group (1-c) and ester group (1-d) being removable from said A 1 by hydrolysis in an acidic aqueous medium having a pH value less than 7, with 2. an organic halide having the general formula Y-X, wherein X is a halogen atom selected from the group consisting of chlorine, bromine and iodine and Y is selected from the group consisting of (2-a) cyclic monovalent nitrogen containing organic radicals and residua free of carbonyl oxygen, and (2-b) monovalent organic radicals and residua having the general formula --R 1 --B, wherein B is selected from the group consisting of ##STR7## --O--R 4 and --S--R 4 , R 1 is a divalent organic radical having a linear carbon chain length of about 1-7 carbon atoms, R 2 and R 3 are selected from the group consisting of --H,--OH, --SH, halogen and monovalent organic radicals and residua having a linear carbon chain length of about 1-7 carbon atoms, R 4 is selected from the group consisting of --H and monovalent organic radicals and residua having a linear carbon chain length of about 1-7 carbon atoms, N is nitrogen, O is oxygen, S is sulfur and H is hydrogen, the said hydrogen atom H of the monosaccharide derivative A 1 -O-H and the said halogen atom X of the organic halide being reactive whereby the said H is replaced by Y to produce an ethereally substituted monosaccharide derivative having the general formula A 1 -O-Y wherein A 1 , Y and O are as above defined, the improvement which comprises reacting said monosaccharide derivative (1) and the said organic halide (2) at an elevated reaction temperature below the thermal decomposition thereof while dissolved in an anhydrous organic solvent in the presence of a solid anhydrous strong inorganic base of a metal selected from the group consisting of the alkali metals and the alkaline earth metals, separating the said ethereally substituted monosaccharide derivative having the general formula A 1 -O-Y from the reaction mixture, and removing at least one but not all of said acetal, ketal or ester groups from A 1 by partial hydrolysis in an acidic aqueous medium having a pH value of about 3-6 to produce an ethereally substituted monosaccharide having the general formula A 2 -O-Y, wherein O and Y are as above defined and A 2 is the residue of a monosaccharide corresponding to A 1 as above defined with at least one but not all of said acetal, ketal or ester groups being removed therefrom.

Claim 9

In a method of preparing an ethereally substituted monosaccharide comprising the steps of reacting 1. a monosaccharide derivative having the general formula A 1 -O-H, wherein O is oxygen, H is hydrogen and A 1 is the residue of a monosaccharide selected from the group consisting of pentoses, hexoses and heptoses which has been derivatized with at least one substance selected from the group consisting of (1-a) at least one alcohol containing 1-18 carbon atoms to produce a hydrolyzable acetal group at the site of at least one available hydroxyl residue, (1-b) at least one aldehyde containing 1-18 carbon atoms to produce at least one hydrolyzable acetal group at the site of at least one available hydroxyl residue, (1-c) at least one ketone containing 1-18 carbon atoms to produce at least one hydrolyzable ketal group at the site of at least one available hydroxyl residue, and (1-d) at least one organic acid residue containing 1-18 carbon atoms to produce a hydrolyzable ester group at the site of at least one available hydroxyl residue, the said hydrolyzable acetal groups (1-a) and (1-b), ketal group (1-c) and ester group (1-d) being removable from said A 1 by hydrolysis in an acidic aqueous medium having a pH value less than 7, with 2. an organic halide having the general formula Y-X, wherein X is a halogen atom selected from the group consisting of chlorine, bromine and iodine and Y is selected from the group consisting of (2-a) cyclic monovalent nitrogen containing organic radicals and residua free of carbonyl oxygen, and (2-b) monovalent organic radicals and residua having the general formula --R 1 --B, wherein B is selected from the group consisting of ##STR7## --O--R 4 and --S--R 4 , R 1 is a divalent organic radical having a linear carbon chain length of about 1-7 carbon atoms, R 2 and R 3 are selected from the group consisting of --H,--OH, --SH, halogen and monovalent organic radicals and residua having a linear carbon chain length of about 1-7 carbon atoms, R 4 is selected from the group consisting of --H and monovalent organic radicals and residua having a linear carbon chain length of about 1-7 carbon atoms, N is nitrogen, O is oxygen, S is sulfur and H is hydrogen, the said hydrogen atom H of the monosaccharide derivative A 1 -O-H and the said halogen atom X of the organic halide being reactive whereby the said H is replaced by Y to produce an ethereally substituted monosaccharide derivative having the general formula A 1 -O-Y wherein A 1 , Y and O are as above defined, the improvement which comprises reacting said monosaccharide derivative (1) and the said organic halide (2) at an elevated reaction temperature below the thermal decomposition thereof while dissolved in an anhydrous organic solvent in the presence of a solid anhydrous strong inorganic base of a metal selected from the group consisting of the alkali metals and the alkaline earth metals, separating the said ethereally substituted monosaccharide derivative having the general formula A 1 -O-Y from the reaction mixture, and removing at least one but not all of said acetal, ketal or ester groups from A 1 by partial hydrolysis in an acidic aqueous medium having a pH value of about 3-6 to produce an ethereally substituted monosaccharide having the general formula A 2 -O-Y, wherein O and Y are as above defined and A 2 is the residue of a monosaccharide corresponding to A 1 as above defined with at least one but not all of said acetal, ketal or ester groups being removed therefrom.

Claim 10

The method of claim 7 wherein the said monosaccharide derivative (1) is selected from the group consisting of glucose derivatives and galactose derivatives.

Claim 11

The method of claim 7 wherein the said monosaccharide derivative (1) is 1,2:5,6-di-O-isopropylidene D-glucofuranose.

Claim 12

The method of claim 9 wherein Y is ##STR8## R 1 is a hydrocarbon radical having a linear carbon chain length of 1-3 carbon atoms, and R 2 and R 3 are selected from the group consisting of hydrogen and hydrocarbon radicals having a linear carbon chain length of 1-3 carbon atoms.

Claim 13

The method of claim 9 wherein Y is selected from the group consisting of -(n-propylamino), (N',N'-dimethylamino-n-propyl), -(N',N'-dimethylaminoisopropyl), -(N-methyl piperidyl), -(N',N'-dimethylaminoethyl), -(N',N'-diethylaminoethyl), and -(2',N',N'-trimethylamino-n-propyl).

Claim 14

The method of claim 9 wherein Y is -(N',N'-dimethylamino-n-propyl).

Claim 15

The method of claim 1 wherein the said monosaccharide derivative (1) has a general formula selected from the group consisting of: ##STR9## wherein Z 1 and Z 2 are selected from the group consisting of --H,--OH, and monovalent hydroxyalkyl, alkoxyl and alkoxyalkyl radicals containing up to 3 carbon atoms, W is selected from the group consisting of H and monovalent alkyl, alkenyl, cyclic alkane, cyclic aromatic, and acyl radicals containing 1-18 carbon atoms, and at least one Z 1 , Z 2 or W is other than --H or --OH the said monosaccharide derivative (1) being selected from the group consisting of glucose derivatives and galactose derivatives, the said glucose derivatives being derivatized in all --OH positions with the exception of the 1-O- or 3-O-position and the said galactose derivatives being derivatized in all --OH positions with the exception of the 6-O position whereby the glucose is ethereally monosubstituted in the 1-O- or 3-O- position and the galactose is ethereally monosubstituted in the 6-O- position, and Y is selected from the group consisting of -(n-propylamino), -(N',N'-dimethylamino-n-propyl), -(N',N'-dimethylaminoisopropyl), -(N-methyl piperidyl), -(N',N'-dimethylaminoethyl), -(N',N'-diethylaminoethyl), and -(2',N',N'-trimethylamino-n-propyl).

Claim 16

The method of claim 1 wherein the said monosaccharide derivative (1) is 1,2:5,6-di-O-isopropylidene-D-glucofuranose and Y is -(N',N'-dimethylamino-n-propyl).

Claim 17

The method of claim 7 wherein the said monosaccharide derivative (1) is selected from the group consisting of glucose derivatives and galactose derivatives, and the glucose derivatives being derivatized in all --OH positions with the exception of the 1-O- or 3-O- positions and the galactose derivatives being derivatized in all --OH positions with the exception of the 6-O- position whereby the glucose is ethereally monosubstituted in the 1-O- or 3-O- position and the galactose is ethereally monosubstituted in the 6-O- position.

Claim 18

The method of claim 7 wherein the said monosaccharide derivative (1) is 1,2:5,6-di-O-isopropylidene-D-glucofuranose and Y is -(N',N'-dimethylamino-n-propyl), and the hydrolysis is performed in a substantially non-oxidizing acidic aqueous medium having a pH value of about 3-6 to remove only one of the said isopropylidene groups.

Claim 19

The method of claim 1 wherein the said organic halide (2) is an amine, and the said amine is initially present in the form of a salt thereof.

Claim 20

The method of claim 1 wherein the said ethereally substituted monosaccharide derivative having the general formula A-O-Y is hydrolyzed to remove at least one of said hydrolyzable acetal, ketal or ester groups from A by hydrolysis in an acidic aqueous medium having a pH value less than 7 to produce an ethereally substituted monosaccharide having the general formula A 3 -O-Y, wherein O and Y are as above defined and A 3 is a residue of a monosaccharide corresponding to A as above defined with at least one of said hydrolyzable acetal, ketal or ester groups being removed therefrom.

Claim 21

The method of claim 18 wherein the said hydrolysis is performed in a substantially non-oxidizing acidic aqueous medium having a pH value less than 3 to remove all of the said hydrolyzable acetal, ketal or ester groups from A.

Claim 22

The method of claim 7 wherein the said organic halide (2) is an amine, and the said amine is initially present in the form of a salt thereof.