Synthesis of diethyl{[5-(3-fluorophenyl)-pyridine-2yl]methyl}phosphonate
View Patent ↗This application discloses a novel process for the preparation of phosphonate esters useful as intermediates in the preparation of himbacine analogs, themselves useful as thrombin receptor antagonists. The chemistry taught herein can be exemplified by the following scheme: wherein R 9 is selected from alkyl, aryl heteroaryl and arylalkyl groups having 1 to 10 carbon atoms, and R 11 is selected independently for each occurrence from alkyl, aryl heteroaryl and arylalkyl groups having 1 to 10 carbon atoms and hydrogen, X 2 is Cl, Br, or I; X 3 is selected from Cl and Br; and PdL n is a supported palladium metal catalyst or a soluble heterogeneous palladium catalyst. The L-derivatizing reagent is a moiety which converts the alcohol functional group of compound 137D to any leaving group which can be displaced by a triorgano-phosphite phosphonating agent.
1. A process for making a compound having the structure of compound 11:
wherein R1 is an alkyl group of from 1 to about 4 carbon atoms, the process comprising:
(a) reacting (5-halo-pyridin-2-yl)-methanol of the Formula 137A
where X 2 is selected independently from Cl, Br, or I;
with an X 1 halogenating agent, to produce a compound of the formula of compound 137,
where X 1 is the same for each occurrence and is selected from Cl or Br and X 2 is as defined above;
(b) reacting compound 137 with a phosphite compound of the structure of Formula A:
wherein R 9 is selected from alkyl, aryl, heteroaryl, and arylalkyl groups having 1 to 10 carbon atoms, to produce compound 138:
wherein R 9 is as defined above;
(c) treating compound 138 with HX 3 , where X 3 is selected from Cl and Br, to precipitate the corresponding hydrohalide salt of Formula 138 A
(d) reacting the hydrohalide salt from step “c” with a 3-flurophenylboronate compound of the structure of Formula B
wherein R 11 is selected independently for each occurrence from alkyl, aryl heteroaryl and arylalkyl groups having 1 to 10 carbon atoms and hydrogen, optionally in the presence of a palladium catalyst to produce compound 116.
2. A process for making a compound having the structure of compound 11:
wherein R1 is an alkyl group of from 1 to about 4 carbon atoms, the process comprising:
(a) reacting (5-Bromo-2-methoxy-pyridine) with a chlorinating agent selected from OSCl 2 , PCl 3 , PCl 5 , to produce a compound of the formula of compound 137;
(b) reacting compound 137 with a phosphite compound of the structure of Formula A
to produce compound 138
wherein R 9 is separately selected for each occurrence from alkyl, aryl, heteroaryl, and arylalkyl groups having 1 to 10 carbon atoms;
(c) treating compound 138 with HCl to obtain the corresponding hydrochloride salt;
(d) reacting the hydrochloride salt from step “c” with 3-flurophenylboronic acid, optionally in the presence of a palladium catalyst to produce compound having the structure of compound 116,
(e) reacting the compound 116 formed in step “d” with a compound of the structure of compound 15,
to yield compound 11.
3. The process of claim 2 wherein the phosphite compound used in step “b” is a trialkyl phosphate.
4. The process of claim 2 wherein the phosphite used in step “b” is triethyl phosphite.
5. The process of claim 1 wherein said palladium catalyst is palladium metal supported on carbon black.
6. The process of claim 1 wherein said palladium catalyst is a soluble palladium catalyst.
7. The process of claim 1 wherein the phosphite used in step “b” is triethyl phosphite.
8. The process of claim 2 wherein said palladium catalyst is selected from palladium metal supported on carbon black and a soluble palladium catalyst.
9. The process of claim 3 wherein said palladium catalyst is selected from palladium metal supported on carbon black and a soluble palladium catalyst.
10. The process of claim 4 wherein said palladium catalyst is selected from palladium metal supported on carbon black and a soluble palladium catalyst.