Process for the preparation of sphingosine derivatives

Claim 2

A process for preparing sphingosine derivatives selected from the formula (I)-D and (I)-L ##STR14## in which R 1 denotes an acyl radical selected from the group consisting of radicals of fatty acids having 14 to 24 carbon atoms and the corresponding acyl radicals having a hydroxyl group in the α-position of having 1 or 2 double bonds in the cis configuration, and R 2 denotes a radical selected from the group consisting of the pentadecanyl and the heptadecanyl radical and the corresponding C 1 5 and C 1 7 radicals having 1, 2 or 3 double bonds, one of which in each case being located in the 1, 2-position and having the trans configuration, the other, or others, when present, having the cis configuration; comprising reacting an optical active compound of the formula (II)-D or (II)-L ##STR15## in which R 1 and R 2 are as defined above, or the corresponding racemate, with an organic reagent which is able selectively to react with a primary hydroxyl group, with the formation of compounds of the formula (III) ##STR16## in which R denotes a hydroxyl protective group, esterifying the compound of the formula (III) with an organic carboxylic acid with the formation of a compound of the formula (IV) ##STR17## in which Ac 1 denotes the acyl radical or an organic carboxylic acid, removing the hydroxyl protective group R from the compounds of the formula (IV) by acid hydrolysis with the formation of corresponding compounds of the formula (VII) ##STR18## reacting the compound of the formula (VII) with the O-trifluoroacetimidate or O-trichloroacetimidate of a D-glucose whose hydroxyl groups in the 2, 3, 4 and 6 positions are protected by acyl radicals Ac 4 in the presence of boron trifluoride etherate or trimethylsiloyl trifluoromethanesulfonate, with the formation of compounds of the corresponding formula (X) ##STR19## separating, if a racemate is used as starting material, into the diastereomers, by chromatography or fractional crystallization, the compound of the formula (X), and eliminating simultaneously the acyl groups Ac 1 and Ac 4 from the compounds of the formula (X), in each case compounds of the D- or L-series being produced from compounds of the D- or L-series, respectively.

Claim 3

A process for the preparation of the sphingosine derivatives of the formula (I)-D or (I)-L ##STR20## in which R 1 denotes an acyl radical selected from the group consisting of radicals of fatty acids having 14 or 24 carbon atoms and the corresponding acyl radicals having a hydroxyl group in the α-position or having 1 or 2 double bonds in the cis configuration, and R 2 denotes a radical selected from the group consisting of the pentadecanyl and the heptadecanyl radical and the corresponding C 1 5 and C 1 7 radicals having 1, 2 or 3 double bonds, one of which in each case being located in the 1,2-position and having the trans configuration, the other, or others, when present, having the cis configuration; which comprises reacting a racemic compound of the formula (II)-D and (II)-L ##STR21## in which R 1 and R 2 , are as defined above, with an organic reagent which is able selectively to react with a primary hydroxyl group, with the formation of compounds of the formula (III) ##STR22## in which R denotes a hydroxyl protective group, esterifying the compound of the formula (III) with an optically active organic acid, and separating into the diastereomers, by chromatography or fractional crystallization, the resulting mixture of diastereomeric compounds of the formula (V) ##STR23## in which Ac 2 denotes the acyl radical of an optically active organic acid, removing the hydroxyl protective group R from the diastereomers of the formula (V) by acid hydrolysis with the formation of corresponding compounds of the formula (VIII) ##STR24## reacting the compound of the formula (VIII) with the O-trifluoroacetimidate or O-trichloroacetimidate of a D-glucose whose hydroxyl groups in the 2, 3, 4 and 6 positions are protected by acyl radicals Ac 4 in the presence of boron trifluoride etherate or trimethylsilyl trifluoromethanesulfonate, with the formation of compounds of the corresponding formula (XI) ##STR25## and eliminating simultaneously the acyl groups Ac 2 and Ac 4 from the compounds of the formula (XI), in each case compounds of the D- or L-series being produced from compounds of the D- L-series respectively.

Claim 4

A process for the preparation of the sphingosine derivatives of the formula (I)-D or (I)-L ##STR20## in which R 1 denotes an acyl radical selected from the group consisting of radicals of fatty acids having 14 or 24 carbon atoms and the corresponding acyl radicals having a hydroxyl group in the α-position or having 1 or 2 double bonds in the cis configuration, and R 2 denotes a radical selected from the group consisting of the pentadecanyl and the heptadecanyl radical and the corresponding C 1 5 and C 1 7 radicals having 1, 2 or 3 double bonds, one of which in each case being located in the 1,2-position and having the trans configuration, the other, or others, when present, having the cis configuration; which comprises reacting a racemic compound of the formula (II)-D and (II)-L ##STR21## in which R 1 and R 2 , are as defined above, with an organic reagent which is able selectively to react with a primary hydroxyl group, with the formation of compounds of the formula (III) ##STR22## in which R denotes a hydroxyl protective group, esterifying the compound of the formula (III) with an optically active organic acid, and separating into the diastereomers, by chromatography or fractional crystallization, the resulting mixture of diastereomeric compounds of the formula (V) ##STR23## in which Ac 2 denotes the acyl radical of an optically active organic acid, removing the hydroxyl protective group R from the diastereomers of the formula (V) by acid hydrolysis with the formation of corresponding compounds of the formula (VIII) ##STR24## reacting the compound of the formula (VIII) with the O-trifluoroacetimidate or O-trichloroacetimidate of a D-glucose whose hydroxyl groups in the 2, 3, 4 and 6 positions are protected by acyl radicals Ac 4 in the presence of boron trifluoride etherate or trimethylsilyl trifluoromethanesulfonate, with the formation of compounds of the corresponding formula (XI) ##STR25## and eliminating simultaneously the acyl groups Ac 2 and Ac 4 from the compounds of the formula (XI), in each case compounds of the D- or L-series being produced from compounds of the D- L-series respectively.

Claim 5

A process for the preparation of the sphingosine derivatives of the formula (I)-D or (I)-L ##STR26## in which R 1 denotes an acyl radical selected from the group consisting of radicals of fatty acids having 14 to 24 carbon atoms and the corresponding acyl radicals having a hydroxyl group in the α-position or having 1 or 2 double bonds in the cis configuration and R 2 denotes a radical selected from the group consisting of the pentadecanyl and the heptadecanyl radical and the corresponding C 1 5 and C 1 7 radicals having 1, 2 or 3 double bonds, one of which in each case being located in the 1,2-position and having the trans configuration, the other, or others, when present, having the cis configuration; comprising reacting a racemic compound of the formula (II)-D and (II)-L ##STR27## in which R 1 and R 2 are as defined above, with an organic reagent which is able selectively to react with a primary hydroxyl group, with the formation of compounds of the formula (III) ##STR28## in which R denotes a hydroxyl protective group, esterifying the compound of the formula (III) with an optically active organic acid, and separating into the diastereomers, by chromatography or fractional crystallization, the resulting mixture of diastereomeric compounds of the formula (V) ##STR29## in which Ac 2 denotes the acyl radical of an optically active organic acid, deacylating the individual diastereomers of the formula (V) and esterifying with an organic carboxylic acid with the formation of enantiomeric compounds of the formula (VI) ##STR30## in which Ac 3 denotes the acyl radical of an organic carboxylic acid, removing the hydroxyl protective group R from the enantiomers of the formula (VI) by acid hydrolysis with the formation of corresponding compounds of the formula (IX) PG,44 ##STR31## reacting the compound of the formula (IX) with the O-trifluoroacetimidate or O-trichloroacetimidate of a D-glucose whose hydroxyl groups in the 2, 3, 4 and 6 positions are protected by acyl radicals Ac 4 in the presence of boron trifluoride etherate or trimethylsilyl trifluoromethanesulfonate, with the formation of compounds of the corresponding formula (XII) ##STR32## and eliminating simultaneously the acyl groups Ac 3 and Ac 4 from the compounds of the formula (XII), in each case compounds of the D- or L-series being produced from compounds of the D- or L-series respectively.

Claim 6

A process for the preparation of the sphingosine derivatives of the formula (I)-D or (I)-L ##STR26## in which R 1 denotes an acyl radical selected from the group consisting of radicals of fatty acids having 14 to 24 carbon atoms and the corresponding acyl radicals having a hydroxyl group in the α-position or having 1 or 2 double bonds in the cis configuration and R 2 denotes a radical selected from the group consisting of the pentadecanyl and the heptadecanyl radical and the corresponding C 1 5 and C 1 7 radicals having 1, 2 or 3 double bonds, one of which in each case being located in the 1,2-position and having the trans configuration, the other, or others, when present, having the cis configuration; comprising reacting a racemic compound of the formula (II)-D and (II)-L ##STR27## in which R 1 and R 2 are as defined above, with an organic reagent which is able selectively to react with a primary hydroxyl group, with the formation of compounds of the formula (III) ##STR28## in which R denotes a hydroxyl protective group, esterifying the compound of the formula (III) with an optically active organic acid, and separating into the diastereomers, by chromatography or fractional crystallization, the resulting mixture of diastereomeric compounds of the formula (V) ##STR29## in which Ac 2 denotes the acyl radical of an optically active organic acid, deacylating the individual diastereomers of the formula (V) and esterifying with an organic carboxylic acid with the formation of enantiomeric compounds of the formula (VI) ##STR30## in which Ac 3 denotes the acyl radical of an organic carboxylic acid, removing the hydroxyl protective group R from the enantiomers of the formula (VI) by acid hydrolysis with the formation of corresponding compounds of the formula (IX) PG,44 ##STR31## reacting the compound of the formula (IX) with the O-trifluoroacetimidate or O-trichloroacetimidate of a D-glucose whose hydroxyl groups in the 2, 3, 4 and 6 positions are protected by acyl radicals Ac 4 in the presence of boron trifluoride etherate or trimethylsilyl trifluoromethanesulfonate, with the formation of compounds of the corresponding formula (XII) ##STR32## and eliminating simultaneously the acyl groups Ac 3 and Ac 4 from the compounds of the formula (XII), in each case compounds of the D- or L-series being produced from compounds of the D- or L-series respectively.

Claim 7

The process as claimed in claim 1, wherein the acyl radical Ac 1 used is that of an aliphatic or aromatic carboxylic acid or a tert.-butoxycarbonyl group.

Claim 8

The process as claimed in claim 4, wherein the acyl radical Ac 1 is the acyl radical or benzoic acid or a substituted benzoic acid.

Claim 9

The process as claimed in claim 1, wherein the hydroxyl protective group R is selected from the group consisting of triphenylmethyl, monomethoxy-triphenylmethyl, tert.-butyl, trichloroacetyl, trimethylsilyl, tert.-butyldimethylosilyl and tert.-butyldiphenylsilyl.

Claim 10

The process as claimed in claim 2, wherein the hydroxyl protective group R is selected from the group consisting of triphenylmethyl, monomethoxy-triphenylmethyl, tert.-butyl, trichloroacetyl, trimethylsilyl, tert.-butyldimethylsilyl and tert.-butyldiphenylsilyl.

Claim 11

The process as claimed in claim 3, wherein the hydroxyl protective group R is selected from the group consisting of triphenylmethyl, monomethoxy-triphenylmethyl, tert.-butyl, trichloroacetyl, trimethylsilyl, tert.-butyldimethylsilyl and tert.-butylodiphenylsilyl.

Claim 12

The process as claimed in claim 3, wherein the acyl radical Ac 3 used is that of an aliphatic or aromatic carboxylic acid or a tert.-butoxycarbonyl group.

Claim 13

The process as claimed in claim 9, wherein the acyl radical Ac 3 is the acyl radical of benzoic acid or a substituted benzoic acid.

Claim 14

The process as claimed in claim 2, wherein the acyl radical Ac 2 used is that of a readily accessible optically active organic acid, selected from the group consisting of tartaric acid, debenzoyltartaric acid, mandelic acid, O-acetylomandelic acid, camphoric acid, camphorsulfonic acid and bromocamphorsulfonic acid.

Claim 15

The process as claimed in claim 1, wherein the acyl radical Ac 4 used is that of an aliphatic or aromatic carboxylic acid.

Claim 16

The process as claimed in claim 2, wherein the acyl radical Ac 4 used is that of an aliphatic or aromatic carboxylic acid.

Claim 17

The process as claimed in claim 3, wherein the acyl radical Ac 4 used is that of an aliphatic or aromatic carboxylic acid.

Claim 18

The process as in claim 12, wherein the acyl radical Ac 4 is the acetyl or benzoyl radical.

Claim 19

The process as in claim 13, wherein the acyl radical Ac 4 is the acetyl or benzoyl radical.

Claim 20

The process as in claim 14, wherein the acyl radical Ac 4 is the acetyl or benzoyl radical.

Claim 21

The process as claimed in claim 1, wherein the elimination of the acyl radicals Ac 1 and Ac 4 in the last stage of the process is carried out by treatment with an alkali metal alcoholate.

Claim 22

The process as claimed in claim 2, wherein the elimination of the acyl radicals Ac 2 and Ac 4 in the last stage of the process is carried out by treatment with an alkali metal alcoholate.

Claim 23

The process as claimed in claim 3, wherein the elimination of the acyl radicals AC 3 and Ac 4 in the last stage of the process is carried out by treatment with an alkali metal alcoholate.

Claim 24

The process as claim in claim 1, wherein the reaction with the trifluoroacetimidate or trichloroacetimidate is carried out in an anhydrous polar solvent.

Claim 25

The process as in claim 2, wherein the reaction with the trifluoroacetimidate or trichloroacetimidate is carried out in an anhydrous polar solvent.

Claim 26

The process as in claim 3, wherein the reaction with the trifluoroacetimidate or trichloroacetimidate is carried out in an anhydrous polar solvent.