Process and intermediates for the synthesis of 2-(quinolin-5-yl)-4,5 disubstituted-azole derivatives

1. A process for preparing an oxazole compound of Formula ID

wherein

R 1 is a haloalkyl;

R 2 , R 4 are alkyl;

R 5 is selected from hydrogen, methyl alkyl, hydroxyalkyl, alkoxyalkyl, mercaptoalkyl, —CH 2 F, —CHF 2 , —CF 3 , —C(O)O-alkyl and —C(O)NR 43a R 44a , where R 43a and R 44a are independently selected for each occurrence from the group of H, alkyl, and a nitrogen protecting group; and

R 6 is selected from acid labile amino protecting groups;

the process comprising:

(a) providing a solution comprising the compound of Formula IDa,

wherein,

R 1 , R 2 and R 4 are defined above;

R 3 is selected from hydrogen and alkyl; and

X is selected from oxygen and sulfur;

(b) reacting the solution provided in Step “a” with an alkali metal amide base; and

(c) reacting the mixture provided in Step “b” with a compound of Formula IDb,

wherein

R 5 and R 6 are as defined above; and

R 7 represents an activated acid moiety.

2. The process of claim 1 wherein R 7 is an alkylcarbonyloxy moiety.

3. The process of claim 1 wherein R 7 is a halogen.

4. The process of claim 2 wherein, Step “b” is carried out by adding an aliquot of an Lewis base in an amount which is less than required to react with all of the compound Formula IDa in a reaction mixture, and Step “c” is carried out by adding an amount of the anhydride compound of Formula IDb equivalent to the amount of the compound of Formula IDa added, then repeating the addition of Lewis base followed by anhydride until substantially all of the compound of Formula IDa has been reacted.

5. A process for preparing the compound of Formula IXab,

the process comprising:

(a) providing the anhydride of Formula Ib1a,

(b) reacting the compound of the Formula Ia1,

with a Lewis base to form an intermediate and reacting that intermediate with the anhydride provided in Step “a” to form the compound of Formula Ia2-ester,

(c) converting the compound of Formula Ia2-ester to the acid of Formula Ia2-acid by treatment with aqueous base;

(d) reacting the compound of Formula Ia2-acid with the amino salt compound of the Formula Ib2a,

to form the compound of Formula Ic2a,

(e) deprotecting the compound of Formula Ic2a formed in Step “d” to form the compound of Formula IXab.

6. The process of claim 5 , wherein the Lewis base is sodium bis(trimethylsilyl)amide (NaHMDS).

7. The process of claim 5 wherein, the aqueous base used in step “c” is 25% sodium hydroxide and hydrolysis is carried out in the presence of ethanol.

8. The process of claim 5 wherein the anhydride of Formula Ib1a in step “a” is prepared by a process comprising reacting the compound of Formula Ib1b (N-Boc-L-alanine),

with trimethylacetylchloride in the presence of dicyclohexylamine.

9. The process of claim 5 wherein the compound of Formula Ib2a used in Step “d”, amidation reaction step, is provided by treating a solution containing a proline derivative compound of the Formula IB2a2,

wherein PG is an acid labile protecting group, with an acid.

10. The process of claim 6 wherein, the aqueous base used in step “c” is 25% sodium hydroxide and hydrolysis is carried out in the presence of ethanol.

11. The process of claim 6 wherein, Step “b” is carried out by placing the compound of Formula Ia1 in a reaction mixture, adding an aliquot of a Lewis base in an amount which is less than required to react with all of the compound of Formula Ia1 present, Step “c” is carried out by adding an amount of the anhydride compound of Formula Ib1 equivalent to the amount of Lewis base added in Step “b”, and repeating the addition of Lewis base followed by anhydride until substantially all of the compound of Formula Ia1 has been reacted.

12. The process of claim 11 wherein the Lewis base is added in from about 5 to about 10 equal aliquots.