Process for preparing bosentan
View Patent ↗The present invention relates to a novel intermediate useful in the preparation of bosentan and to processes for the preparation of said intermediate and bosentan. The invention further relates to compositions comprising bosentan prepared according to the processes of the invention and their use in the treatment of endothelin-receptor mediated disorders.
1. A process for preparing bosentan comprising:
(a) reacting a dichloro compound of formula (1) with a mono-protected ethylene glycol of formula HOCH 2 CH 2 OR, wherein R is a hydroxyl protecting moiety, to afford a compound of formula (2a):
(b) coupling compound (2a) with 4-tert-butyl phenyl sulfonamide;
(c) removing the protecting moiety R; and
(d) isolating bosentan from the mixture obtained in step (c).
2. A process according to claim 1 , wherein R is selected from the group consisting of alkyl, aryl, arylalkyl, allyl, silyl, benzoate, pivalate and t-butyl.
3. A process according to claim 1 , wherein in step (a) the dichloro compound of formula (1) and the mono-protected ethylene glycol are reacted in the presence of a base selected from the group consisting of sodium metal, DBU, DBN, DMAP, pyridine, lithium hydroxide and sodium hydroxide.
4. A process according to claim 1 , wherein step (a) is carried out in an organic solvent selected from the group consisting of toluene, THF, xylene, DMF, DMSO, acetonitrile and dimethylacetamide.
5. A compound having the structure as shown in formula (2a) or a salt or crystalline form thereof:
wherein R is a hydroxyl protecting moiety.
6. A compound according to claim 5 , wherein R is selected from the group consisting of alkyl, aryl, arylalkyl, allyl, silyl, benzoate, pivalate and tert-butyl.
7. A compound according to claim 5 , wherein the salt is selected from the group consisting of a tartrate, succinate, oxalate, pimelate, adipate, acetate, suberate, salicylate, mesylate, malate, malonate, maleate, camphorsulfonate, mandelate, hydrochloride, hydrogen sulfate, sulfate, hydrobromide, besylate, benzoate, dihydrogen phosphate, glutarate, and citrate salt.
8. A process for preparing a compound of formula (2a) comprising coupling a dichloro compound of formula (1) to a mono-protected ethylene glycol of formula HOCH 2 CH 2 OR, wherein R is a hydroxyl protecting moiety, to afford a compound of formula (2a):
9. A process according to claim 8 , wherein R is selected from the group consisting of alkyl, aryl, arylalkyl, allyl, silyl, benzoate, pivalate and tert-butyl.
10. A process according to claim 8 , wherein the dichloro compound of formula (1) is coupled to the mono-protected ethylene glycol in the presence of a base selected from the group consisting of sodium metal, DBU, DBN, DMAP, pyridine, lithium hydroxide and sodium hydroxide.
11. A process according to claim 8 , wherein the reaction mixture is heated to between about 30-90° C.
12. The process according to claim 1 , wherein in step (a) the dichloro compound of formula (1) and the mono-protected ethylene glycol are reacted in the presence of a base selected from the group consisting of alkali metal hydroxides and alkaline earth metal hydroxides.
13. The process according to claim 1 , wherein the reaction mixture in step (a) is heated to between about 30-90° C.
14. The process according to claim 13 , wherein the reaction mixture in step (a) is heated to between about 50-60° C.
15. The process according to claim 1 , wherein the bosentan is isolated in step (d) by filtration and then dried under reduced pressure until a constant weight is achieved.
16. The process according to claim 8 , wherein the dichloro compound of formula (1) is coupled to the mono-protected ethylene glycol in the presence of a base selected from the group consisting of alkali metal hydroxides and alkaline earth metal hydroxides.
17. The process according to claim 8 , wherein the dichloro compound of formula (1) is coupled to the mono-protected ethylene glycol in the presence of an organic solvent selected from the group consisting of toluene, THF, xylene, DMF, DMSO, acetonitrile, and dimethylacetamide.
18. The process according to claim 11 , wherein the reaction mixture is heated to between about 50-60° C.