Process for the preparation of taxol and 10-deacetyltaxol

Claim 2

A process for the preparation of a taxane of the formula ##STR16## wherein R 1 is C 6 H 5 or ##STR17## and R 2 is hydrogen or acetyl, which comprises the steps of: (a) reacting a periodate with a taxane-7-xyloside of the formula: ##STR18## wherein R 1 and R 2 are as defined in a reaction-inert solvent at a temperature of from about 0° to about 60° C.; and (b) reacting the products obtained in step (a) with phenylhydrazine and acetic acid in a reaction-inert solvent at a temperature of from about 20° to about 60° C.

Claim 3

The process according to claim 1, wherein the periodate used in step (a) is sodium periodate.

Claim 4

The process according to claim 1, wherein step (a) is carried out at room temperature.

Claim 5

The process according to claim 1, further comprising the step of acetylating the compound of formula (I) wherein R 2 is hydrogen to produce the compound of formula (I) wherein R is acetyl.

Claim 6

The process according to claim 4, wherein prior to the step of acetylation the 7- and 2'-hydroxyls of the compound is protected and after the acetylation the 7- and the 2'-hydroxyl is deprotected.

Claim 7

The process according to claim 5, wherein the acetylation is carried out by contacting the compound with acetic anhydride in the presence of pyridine at a temperature of about 0° to 100° C.

Claim 8

A process for the preparation of a taxane of the formula ##STR19## wherein R 3 is C 6 H 5 or ##STR20## and R 4 is hydrogen or acetyl, which comprises the steps of: (a) reacting a periodate with a taxane-7-xyloside of the formula: ##STR21## wherein R 3 is as defined in a reaction-inert solvent at a temperature from about 0° to about 60° C.; (b) reacting the products obtained in step (a) with an acetylating, agent in a reaction-inert solvent; and (c) reacting the acetylated products obtained in step (b) with phenylhydrazine and acetic acid in a reaction-inert solvent at a temperature of from about 20° to about 60° C.

Claim 9

A process for the preparation of a taxane of the formula ##STR19## wherein R 3 is C 6 H 5 or ##STR20## and R 4 is hydrogen or acetyl, which comprises the steps of: (a) reacting a periodate with a taxane-7-xyloside of the formula: ##STR21## wherein R 3 is as defined in a reaction-inert solvent at a temperature from about 0° to about 60° C.; (b) reacting the products obtained in step (a) with an acetylating, agent in a reaction-inert solvent; and (c) reacting the acetylated products obtained in step (b) with phenylhydrazine and acetic acid in a reaction-inert solvent at a temperature of from about 20° to about 60° C.

Claim 10

The process according to claim 7, wherein the periodate used in step (a) is sodium periodate.

Claim 11

The process according to claim 7, wherein step (a) is carried out at room temperature.

Claim 12

The process according to claim 7, wherein the acetylating agent is acetic anhydride.

Claim 13

The process according to claim 10, wherein the reaction-inert solvent used in step (b) is pyridine.

Claim 14

The process according to claim 7, wherein step (b) is carried out at about 0° to 100° C.

Claim 15

The process according to claim 7, further comprising the step of deacetylating the compound of formula (III) wherein R 4 is acetyl to produce the compound of formula (III) wherein R 4 is hydrogen.

Claim 16

The process according to claim 13, wherein the deacetylation is carried out by contracting the compound of formula (III) wherein R 4 is acetyl with dimethylamine in methanol.

Claim 17

A process for the preparation of a taxane of the formula: ##STR22## wherein R 5 is C 6 H 5 ir ##STR23## R 6 is an acyl selected from the group consisting of benzoyl, butyryl, carbobenzoxyalanyl, propionyl, succinyl, and trifluoroacetyl or hydrogen; and R 7 is an acyl selected from the group consisting of benzoyl, butyryl, carbobenzoxyalanyl, propionyl, succinyl, and trifluoroacetyl, with the proviso that when R 6 is an acyl, R 6 and R 7 are the same, which comprises the steps of: (a) reacting a periodate with a taxane-7-xyloside of the formula: ##STR24## wherein R 3 is C 6 H 5 or ##STR25## in a reaction-inert solvent at a temperature of from about 0° to about 60° C.; (b) reacting the products obtained in step (a) with an acylating agent in a reaction-inert solvent; and (c) reacting the acylated products obtained in step (b) with phenylhydrazine and acetic acid in a reaction-inert solvent at a temperature of from about 20° to 60° C.

Claim 18

A process for the preparation of a taxane of the formula: ##STR22## wherein R 5 is C 6 H 5 ir ##STR23## R 6 is an acyl selected from the group consisting of benzoyl, butyryl, carbobenzoxyalanyl, propionyl, succinyl, and trifluoroacetyl or hydrogen; and R 7 is an acyl selected from the group consisting of benzoyl, butyryl, carbobenzoxyalanyl, propionyl, succinyl, and trifluoroacetyl, with the proviso that when R 6 is an acyl, R 6 and R 7 are the same, which comprises the steps of: (a) reacting a periodate with a taxane-7-xyloside of the formula: ##STR24## wherein R 3 is C 6 H 5 or ##STR25## in a reaction-inert solvent at a temperature of from about 0° to about 60° C.; (b) reacting the products obtained in step (a) with an acylating agent in a reaction-inert solvent; and (c) reacting the acylated products obtained in step (b) with phenylhydrazine and acetic acid in a reaction-inert solvent at a temperature of from about 20° to 60° C.

Claim 19

The process according to claim 15, further comprising the step of deacylating the compound of formula (V) wherein R 6 is acyl to produce the compound of formula (V) wherein R 6 is hydrogen.

Claim 20

The process according to claim 16, wherein the deacylation is carried out by contracting the compound of formula (V) wherein R 6 is acyl with dimethylamine in methanol.

Claim 21

The process according to claim 15 wherein R 7 is succinyl.