Process
The present invention relates to a process for the preparation of S-[2-[1-(2 -ethylbutyl)cyclohexylcarbonylamino]-phenyl] 2-methylthiopropionate which is useful as a pharmaceutically active compound.
1. A process for the preparation of a compound of formula (Ia):
wherein R 1 is a (C 1 -C 8 ) aryl, Which comprises reacting a compound of formula (II′):
wherein R is H or a compound of the formula:
with H 2 in the presence of (1) an acylating agent anhydride derivative [((C 1 -C 8 )alkyl)C(═O)] 2 or [aryl(C═O)] 2 O or a halide derivative ((C 1 -C 8 )alkyl)C(═O)halide or aryl(C═O) halide and (2) a heterogeneous transition metal hydrogenation catalyst.
2. A process for the preparation of a compound of formula (Ia) and Formula (X):
wherein R 1 is a (C 1 -C 8 ) aryl, Which comprises reacting a compound of formula (II′):
wherein R is H or a compound of the formula:
with H 2 in the presence of (1) an acylating agent anhydride derivative [((C 1 -C 8 )alkyl)C(═O)] 2 or [aryl(C═O)] 2 O or a halide derivative ((C 1 -C 8 )alkyl)C(═O)halide or aryl(C═O)halide and (2) a heterogeneous transition metal hydrogenation catalyst.
3. The process according to claim 2 , wherein R is:
4. The process according to claim 1 wherein R 1 is isopropyl and the acylating agent is isobutyric anhydride or isobutyryl halide.
5. The process according to claim 1 wherein the acylating agent is isobutyric anhydride.
6. The process according to claim 5 , wherein 2.0 to 4.0 equivalents of is obutyric anhydride with respect to the disulfide of formula (II′) is used.
7. The process according to claim 1 , wherein said process is performed in the presence of a solvent or a mixture of two or more solvents.
8. The process according to claim 7 , wherein the solvent is an organic solvent.
9. The process according to claim 7 , wherein the solvent is an ether like solvent, ester like solvent, aliphatic hydrocarbon solvent, saturated alicyclic hydrocarbon solvent, aromatic solvent or a mixture thereof.
10. The process according to claim 7 , wherein the solvent is an aliphatic hydrocarbon solvent, saturated alicyclic hydrocarbon solvent, or aromatic solvent.
11. ihe process according to claim 1 , wherein the acylatmg agent is an anhydride derivative which can act as a solvent or co-solvent with a molar ratio anhydride/amidodisulfide of 2 to 19.
12. The process according to claim 1 , wherein the H 2 is added at a pressure of at least 0.1 bar.
13. The process according to cliam 1 , wherein the reaction is carried out at temperature up to 150° C.
14. The process according to claim 1 , wherein the heterogeneous transition metal hydrogenation catalyst is a Raney catalyst, Pd/C, Pd(OH) 2 /C, Nanoparticulate Palladium(0) microencapsulated in polyurea matrix, Au/TiO 2 , Rh/C, Ru/Al 2 O 3 , Ir/CaCo 3 , Pt/C, or a mixture thereof.
15. The process according to claim 1 , wherein the heterogeneous transition metal hydrogenation catalyst is a Raney catalyst, Pd/C, Pd(OH) 2 /C, Au/TiO 2 , Rh/C, Ru/Al 2 O 3 , Ir/CaCO 3 , Pt/C, or a mixture thereof.
16. The process according to claim 1 , wherein the heterogeneous transition metal hydrogenation catalyst is Pd/C, Pd(OH) 2 /C, Au/TiO 2 , Rh/C, Ra—Ni or Pt/C.
17. The process according to claim 1 , wherein the heterogeneous transition metal hydrogenation catalyst is Pd/C or Ra—Ni.