Granted Patent B2

US 9,981,978 · App. 14/906,776 · Granted May 29, 2018

Abstract

Claims (98)

1. A process for the preparation of a compound of formula I,

wherein:

R 1 represents hydrogen, C 1-18 alkyl, C 2-18 alkenyl, C 2-18 alkynyl or C 3-18 cycloalkyl, (which latter four groups are optionally substituted by one or more halo atoms) or a suitable hydroxy protecting group;

R 2 represents hydrogen or C 1-18 alkyl, C 2-18 alkenyl, C 2-18 alkynyl or C 3-18 cycloalkyl, (which latter four groups are optionally substituted by one or more halo atoms), or a suitable nitrogen protecting group; and

R 3 represents hydrogen, —OH, C 1-18 alkyl, C 1-18 alkoxy, C 2-18 alkenyl, C 2-18 alkynyl, C 3-18 cycloalkyl, (which latter five groups are optionally substituted by one or more halo atoms) or —OR P wherein R P is a suitable hydroxy protecting group;

which process comprises contacting a compound of formula II,

wherein R 1a , R 2a and R 3a are defined according to R 1 , R 2 and R 3 , respectively,

with:

(i) a rhodium complex; and

(ii) an organic additive selected from the group consisting of:

(a) alcohols of formula IIIa,

wherein R x1 , R x2 and R x3 independently represent hydrogen, a C 1-6 alkyl group, a C 2-6 alkenyl group, an aryl group or a heteroaryl group (which latter four groups may be optionally substituted by one or more halo atoms or C 1-4 alkyl groups); or

any two of R x1 , R x2 and R x3 are linked together, along with the requisite carbon atom to which they are attached, to form a 4- to 8-membered cyclic alcohol, optionally containing one or more unsaturated bonds within the ring, and which ring is optionally substituted by one or more halo atoms or C 1-4 alkyl groups;

(b) ketones of formula IIIb,

wherein R x4 and R x5 independently represent a C 1-4 alkyl group, a C 2-4 alkenyl group, an aryl group or a heteroaryl group (which four groups may be optionally substituted by one or more halo atoms or C 1-4 alkyl groups); or

R x4 and R x5 are linked together, along with the requisite carbon atom to which they are attached, to form a 4- to 8-membered cyclic ketone, optionally containing one or more unsaturated bonds within the ring, and which ring is optionally substituted by one or more halo atoms or C 1-4 alkyl groups;

(c) ethers of formula IIIc,

wherein R x6 and R x7 independently represent a C 1-4 alkyl group, or a C 2-4 alkenyl group (which groups may be optionally substituted by one or more halo atoms or C 1-4 alkyl groups); or

R x6 and R x7 are linked together, along with the requisite oxygen atom to which they are attached, to form a 4- to 7-membered cyclic ether, optionally containing one or more unsaturated bonds within the ring, and which ring is optionally substituted by one or more halo atoms or C 1-4 alkyl groups; and

(d) thioethers of formula IIId,

wherein R x8 and R x9 independently represent a C 1-4 alkyl group, or a C 2-4 alkenyl group (which groups may be optionally substituted by one or more halo atoms or C 1-4 alkyl groups); or

R x8 and R x9 are linked together, along with the requisite sulfur atom to which they are attached, to form a 4- to 7-membered cyclic thioether, optionally containing one or more unsaturated bonds within the ring, and which ring is optionally substituted by one or more halo atoms or C 1-4 alkyl groups,

wherein the rhodium complex is water-soluble, and prepared from a water-soluble phosphine and a precursor rhodium complex of formula IV,

[Rh(diene)L n ] + X −   IV

or a dimer of formula V,

[Rh(diene)(Hal)] 2   V

wherein diene represents a diene ligand, X represents an anion, L represents a neutral ligand, n represents 1 to 3, and Hal represents a halide or a hydroxide,

and wherein, when the rhodium complex is prepared from the water-soluble phosphine and the dimer of formula V, the rhodium complex is formed in the presence of a salt of formula AY, wherein A represents an organic or inorganic cation, and Y represents a non-coordinating anion, and

wherein the conversion of the compound of formula II to the compound of formula I is performed in an aqueous solvent system.

2. The process as claimed in claim 1 , wherein R 3 represents hydrogen and R 2 represents methyl.

3. The process as claimed in claim 1 , wherein R 3 represents hydrogen, R 2 represents methyl and R 1 represents hydrogen or methyl.

4. The process as claimed in claim 1 , wherein the organic additive is:

(a) a compound of formula IIIa, as defined in claim 1 , wherein R x1 , R x2 and R x3 each independently represents hydrogen, a C 1-4 alkyl group, a C 6-10 aryl group or a 5- to 10-membered heteroaryl group (which latter three groups may be optionally substituted by one or more halo atoms or C 1-4 alkyl groups);

(b) a compound of formula IIIb, as defined in claim 1 , wherein R x4 and R x5 each independently represents a C 1-4 alkyl group, a C 6-10 aryl group or a 5- to 10-membered heteroaryl group (which three groups may be optionally substituted by one or more halo atoms or C 1-4 alkyl groups);

(c) a compound of formula IIIc, as defined in claim 1 , wherein R x6 and R x7 are linked together, along with the requisite oxygen atom to which they are attached, to form a 5- to 6-membered cyclic ether (which ring may be optionally substituted by one or more halo atoms or methyl groups); or

(d) a compound of formula IIId, as defined in claim 1 , wherein R x8 and R x9 independently represent a C 1-4 alkyl group, or a C 2-4 alkenyl group (which groups may be optionally substituted by one or more halo atoms or C 1-4 alkyl groups).

5. The process as claimed in claim 4 , wherein the organic additive is tert-butanol, isopropanol or acetone.

6. The process as claimed in claim 1 , wherein the compound of formula II is brought into contact with the organic additive before the compound of formula II is brought into contact with the rhodium complex.

7. The process as claimed in claim 1 , wherein:

(i) the compound of formula II is provided in the aqueous solvent system;

(ii) the organic additive is added to the mixture of a compound of formula II and the aqueous solvent system; and then

(iii) the water-soluble phosphine and the precursor rhodium complex are added to the mixture comprising the compound of formula II, the organic additive and the aqueous solvent system.

8. The process as claimed in claim 1 , wherein the organic additive is added in an amount of from 1 to 20 equivalents relative to the amount of the compound of formula II.

9. The process as claimed in claim 1 , wherein the aqueous solvent comprises from 30% to 60% by weight of water.

10. The process as claimed in claim 1 , wherein the process is performed at a temperature of greater than about 60° C.

11. The process as claimed in claim 1 , wherein:

(i) the rhodium complex is pre-formed from the water-soluble phosphine and the precursor rhodium complex prior to addition to the compound of formula II; or

(ii) the rhodium complex is formed from the water-soluble phosphine and the precursor rhodium complex in the presence of the compound of formula II.

12. The process as claimed in claim 11 , wherein the precursor rhodium complex is a compound of formula IVA;

[Rh(diene)(CH 3 CN) 2 ] + X −   IVA

wherein diene represents a diene ligand, and X represents a suitable anion.

13. The process as claimed in claim 11 , wherein the water-soluble phosphine is a compound of formula VI,

P(R 4 )(R 5 )(R 6 )  VI

wherein each of R 4 , R 5 and R 6 independently represents a C 1-6 alkyl or an aryl group, both of which groups may be optionally substituted by one or more groups selected from the list consisting of —OR 6a , —SO 2 OH, C(O)R 7a , —N(R 8a )R 9a , or a salt of —SO 2 OH or —N(R 8a )R 9a ;

or any two of R 4 , R 5 and R 6 may be linked together to form a 4- to 7- (e.g. 5- to 6-) membered ring, optionally containing one or more heteroatoms (for example, in addition to the phosphorus atom that is already present, one or more heteroatoms selected from oxygen, nitrogen and sulfur) and which ring is optionally substituted by one or more substituents selected from —OR 6b , —SO 2 OH, C(O)R 7b , —N(R 8b )R 9b , or a salt of —SO 2 OH or —N(R 8b )R 9b ;

or all three of R 4 , R 5 and R 6 may be linked together to form a cage-like structure (e.g. having an adamantane-type skeleton) optionally containing one or more heteroatoms (for example, in addition to the phosphorus atom that is already present, one or more heteroatoms selected from oxygen, nitrogen and sulfur), and which cage-like structure is optionally substituted by one or more substituents selected from —OR 6c , —SO 2 OH, C(O)R 7c , —N(R 8c )R 9c , or a salt of —SO 2 OH or —N(R 8c )R 9c ;

wherein R 6a , R 6b , R 6c , R 7a , R 7b , R 7c , R 8a , R 8b , R 8c , R 9a R 9b , and R 9c are each independently selected from hydrogen, and C 1-4 alkyl.

14. The process as claimed in claim 1 , wherein the rhodium complex is a complex formed by reacting [Rh(COD)(CH 3 CN) 2 ](BF 4 ) with 1,3,5-triaza-7-phosphaadamantane, wherein COD represents 1,5-cyclooctadiene.

15. A process for the preparation of a compound of formula I,

wherein:

R 1 represents hydrogen, C 1-4 alkyl (which latter group is optionally substituted by one or more halo atoms) or a suitable hydroxy protecting group;

R 2 represents hydrogen or C 1-4 alkyl, (which latter group is optionally substituted by one or more halo atoms), or a suitable nitrogen protecting group; and

R 3 represents hydrogen, —OH, C 1-4 alkyl, C 1-4 alkoxy (which latter two groups are optionally substituted by one or more halo atoms) or —OR P wherein R P is a suitable hydroxy protecting group;

which process comprises contacting a compound of formula II,

wherein R 1a , R 2a and R 3a are defined according to R 1 , R 2 and R 3 , respectively;

with:

(i) a rhodium complex, and

(ii) an organic additive that is:

(a) a compound of formula IIIa, as defined in claim 1 , wherein R x1 , R x2 and R x3 each independently represents hydrogen, a C 1-4 alkyl group, a C 6-10 aryl group or a 5- to 10-membered heteroaryl (which latter three groups may be optionally substituted by one or more halo atoms or C 1-4 alkyl groups);

(b) a compound of formula IIIb, as defined in claim 1 , wherein R x4 and R x5 each independently represents a C 1-4 alkyl group, a C 6-10 aryl group or a 5- to 10-membered heteroaryl group (which three groups may be optionally substituted by one or more halo atoms or C 1-4 alkyl groups);

(c) a compound of formula IIIc, as defined in claim 1 , wherein R x6 and R x7 are linked together, along with the requisite oxygen atom to which they are attached, to form a 5- to 6-membered cyclic ether (which ring may be optionally substituted by one or more halo atoms or methyl groups); or

(d) a compound of formula IIId, as defined in claim 1 , wherein R x8 and R x9 independently represent a C 1-4 alkyl group, or a C 2-4 alkenyl group (which groups may be optionally substituted by one or more halo atoms or C 1-4 alkyl groups);

wherein the organic additive is present in an amount of from 1 to 20 equivalents relative to the compound of formula II, and the conversion of the compound of formula II to the compound of formula I is performed in an aqueous solvent system,

wherein the rhodium complex is water-soluble, and prepared from a water-soluble phosphine and a precursor rhodium complex of formula IV,

[Rh(diene)L n ] + X −   IV

or a dimer of formula V,

[Rh(diene)(Hal)] 2   V

wherein diene represents a diene ligand, X represents an anion, L represents a neutral ligand, n represents 1 to 3, and Hal represents a halide or a hydroxide,

and wherein, when the rhodium complex is prepared from the water-soluble phosphine and the dimer of formula V, the rhodium complex is formed in the presence of a salt of formula AY, wherein A represents an organic or inorganic cation, and Y represents a non-coordinating anion.

16. A process for the preparation of a compound of formula I,

wherein:

R 1 represents hydrogen or methyl;

R 2 represents methyl;

R 3 represents hydrogen;

which process comprises contacting a compound of formula II,

wherein R 1a , R 2a and R 3a are defined according to R 1 , R 2 and R 3 , respectively;

with a rhodium complex, and tert-butanol,

wherein the rhodium complex is prepared from a water-soluble phosphine and [Rh(COD)(CH 3 CN) 2 ](BF 4 ), and the conversion of the compound of formula II to the compound of formula I is performed in an aqueous solvent system that comprises from 30% to 60% water by weight or by volume, wherein COD represents 1,5-cyclooctadiene.

17. The process as claimed in claim 1 , which comprises a further processing step following the conversion of the compound of formula II to the compound of formula I, wherein the further processing step is a recrystallisation step.

18. The process as claimed in claim 1 , which comprises the additional step of crystallisation of the compound of formula I from a solvent system.

19. A process for preparing a salt of a compound of formula I, as defined in claim 1 , which process comprises the steps of:

(i) preparing a compound of formula I in accordance with the process as defined in claim 1 ;

(ii) optionally isolating and/or purifying the compound of formula I obtained from that process; and

(iii) bringing into association the compound of formula I so formed with an organic acid.

20. A process for preparing a pharmaceutical formulation comprising a compound of formula I, or a salt thereof, as defined in claim 1 , which process is characterised in that it includes as a process step a process as claimed in claim 1 followed by bringing into association the compound of formula I (or a salt thereof) so formed, with one or more pharmaceutically-acceptable excipients, adjuvants, diluents or carriers.

21. The process as claimed in claim 1 , wherein the aqueous solvent comprises at least 20% by weight of water.

22. The process as claimed in claim 1 , wherein A is triphenyl carbenium, Ag + , Na + , K + or Li + ; and Y is tetrakis(polyfluoroaryl)borate, SbF 6 − , BF 4 − , ClO 4 − , PF 6 − , HSO 4 − , H 2 PO 4 − , CH 3 CO 2 − , CF 3 CO 2 − , CF 3 SO 3 − or PhCO 2 − .

23. The process as claimed in claim 1 , wherein diene is 1,5-cyclooctadiene, bicyclo[2,2,1]heptadiene or norbornadiene, X is halide, tetrakis(polyfluoroaryl)borate, SbF 6 − , BF 4 − , ClO 4 − , PF 6 − , HSO 4 − , H 2 PO 4 − , CH 3 CO 2 − , CF 3 CO 2 − , CF 3 SO 3 − or PhCO 2 − , and L is acetonitrile, acetone, dimethyl formamide, tetrahydrofuran, dimethyl sulfoxide or benzonitrile.

Assignments (10)