Method for the preparation of fluticasone and related 17β-carbothioic esters using a novel carbothioic acid synthesis and novel purification methods
View Patent ↗This invention discloses a novel method for the conversion of carboxylic acids to carbothioic acids and application of the method to the preparation of androstane carbothiolates, such as fluticasone propionate, which avoids column chromatography.
1. A method for the preparation of a compound of formula (7)
wherein the symbol
represents a single bond or a double bond; one of R 1 or R 2 is hydrogen and the other is optionally protected hydroxyl; or R 1 and R 2 together are oxo; R 3 and R 4 are independently hydrogen or halide; and R 5 and R 6 are independently C 1 –C 6 alkyl; the method comprising:
(c) reacting a compound of formula (3)
and a first base, an iodide salt, and the compound of formula (4)
wherein R 7 and R 8 are independently C 1 –C 6 alkyl; or R 7 and R 8 together are C 1 –C 6 alkaline, in a solvent comprising 2-butanone and water, the water present in about one quarter percent by weight to about ten percent by weight of the compound of formula (3)
to provide a compound of formula (5)
(d) reacting the product of step (c) and NaSH to provide a compound of formula (6)
(e) reacting the product of step (d) and acid;
(f) reacting the product of step (e) and chlorofluoromethane optionally in the presence of a second base;
and
(g) optionally deprotecting the product of step (f).
2. The method of claim 1 , wheiein the first base is a carbonate salt, an amine, or a mixture thereof.
3. The method of claim 1 , wherein the iodide salt is an alkali metal iodide, an alkali earth metal iodide, or a tetraalkylammonium iodide.
4. The method of claim 1 , wherein the second base is a carbonate salt.
5. A method for the preparation of a compound of formula (7)
wherein the symbol
represents a single bond or a double bond; one of R 1 or R 2 is hydrogen and the other is optionally protected hydroxyl; or R 1 and R 2 together are oxo; R 3 and R 4 are independently hydrogen or halide; and R 5 and R 6 are independently C 1 –C 6 alkyl; the method comprising:
(b) reacting a compound of formula (2)
and an alkanoyl halide and the first base to provide the compound of formula (3)
(c) reacting a compound of formula (3)
and a first base, an iodide salt, and a compound of formula (4)
wherein R 7 and R 8 are independently C 1 –C 6 alkyl; or R 7 and R 8 together are C 1 –C 6 alkaline, in a solvent comprising 2-butanone and water, the water present in about one quarter percent by weight to about ten percent by weight of the compound of formula (3) to provide a compound of formula (5)
(d) reacting the product of step (c) and NaSH to provide a compound of formula (6)
(e) reacting the product of step (d) and acid;
(f) reacting the product of step (e) and chlorofluoromethane optionally in the presence of a second base; and
(g) optionally deprotecting the product of step (f).
6. A method for the preparation of a compound of formula (7)
wherein the symbol
represents a single bond or a double bond; one of R 1 or R 2 is hydrogen and the other is optionally protected hydroxyl; or R 1 and R 2 together are oxo; R 3 and R 4 are independently hydrogen or halide; and R 5 and R 6 are independently C 1 –C 6 alkyl; the method comprising:
(c) reacting a compound of formula (3)
and a first base, an iodide salt, and the compound of formula (4)
wherein R 7 and R 8 are independently C 1 –C 6 alkyl; or R 7 and R 8 together are C 1 –C 6 alkaline, in a solvent comprising 2-butanone and water, the water present in about one quarter percent by weight to about ten percent by weight of the compound of formula (3)
to provide a compound of formula (5)
(d) reacting the product of step (c) and NaSH to provide a compound of formula (6)
(e) reacting the product of step (d) and chlorofluoromethane;
and
(f) optionally deprotecting the product of step (e).
7. A method for the preparation of a compound of formula (7)
wherein the symbol
represents a single bond or a double bond; one of R 1 or R 2 is hydrogen and the other is optionally protected hydroxyl; or R 1 and R 2 together are oxo; R 3 and R 4 are independently hydrogen or halide; and R 5 and R 6 are independently C 1 –C 6 alkyl; the method comprising:
(b) reacting a compound of formula (2)
and an alkanoyl halide and the first base to provide the compound of formula (3)
(c) reading a compound of formula (3)
and a first base, an iodide salt, and a compound of formula (4)
wherein R 7 and R 8 are independently C 1 –C 6 alkyl; or R 7 and R 8 together are C 1 –C 6 alkaline, in a solvent comprising 2-hutanone and water, the water present in about one quarter percent by weight to about ten percent by weight of the compound of formula (3) to provide a compound of formula (5)
(d) reacting the product of step (c) and NaSH to provide a compound of formula (6)
(e) reacting the product of step (d) and chlorofluoromethane; and
(f) optionally deprotecting the product of step (e).