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 of the structure of compound 116
wherein R 9 is separately selected for each occurrence from alkyl, aryl, heteroaryl, and arylalkyl groups having 1 to 10 carbon atoms, the process comprising:
reacting a hydrochloride salt compound having the structure of compound 139, where R 9 is as defined above,
with 3-fluorophenylboronic acid in the presence of a palladium catalyst.
2. The process of claim 1 wherein compound 139 is provided by
(a) reacting the hydrochloride salt of the structure of compound 137
with a phosphite compound of the structure of Formula A
wherein R 9 is separately selected for each occurrence from alkyl, aryl, heteroaryl, and arylalkyl groups having 1 to 10 carbon atoms; and
(b) treating the reaction product from step “a” with HCl to obtain compound 139.
3. The process of claim 2 wherein the phosphite compound used in step “a” is a trialkyl phosphite.
4. The process of claim 3 wherein the trialkyl phosphite used in step “a” is triethyl phosphite.
5. The process of claim 1 wherein said palladium catalyst is palladium metal supported on carbon black or a soluble palladium catalyst.
6. The process of claim 2 wherein said palladium catalyst is palladium metal supported on carbon black or a soluble palladium catalyst.
7. The process of claim 3 wherein said palladium catalyst is palladium metal supported on carbon black or a soluble palladium catalyst.
8. The process of claim 4 wherein said palladium catalyst is palladium metal supported on carbon black or a soluble palladium catalyst.
9. The process claim 2 further comprising after the “treating” step “b”, the step of precipitating the phosphonate hydrochloride formed in step “b” by adding an antisolvent to the reaction mixture containing the phosphonate hydrochloride compound of structure 139.
10. The process claim 3 further comprising after the “treating” step “b”, the step of precipitating the phosphonate hydrochloride formed in step “b” by adding an antisolvent to the reaction mixture containing the phosphonate hydrochloride compound of structure 139.
11. The process claim 4 further comprising after the “treating” step “b”, the step of precipitating the phosphonate hydrochloride formed in step “b” by adding an antisolvent to the reaction mixture containing the phosphonate hydrochloride compound of structure 139.
12. The process of claim 6 further comprising, after the “treating” step “b”, the step of precipitating the phosphonate hydrochloride formed in step “b” by adding an antisolvent to the reaction mixture containing the phosphonate hydrochloride compound of structure 139.
13. A process for making a compound of the structure of compound 116
wherein R 9 is separately selected for each occurrence from alkyl, aryl, heteroaryl, and arylalkyl groups having 1 to 10 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 138A,
wherein R 9 is as defined above; and
(d) reacting the hydrohalide salt from step “c” with a 3-fluorophenylboronate 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.
14. A process for making a compound of the structure of compound 116
wherein R 9 is separately selected for each occurrence from alkyl, aryl, heteroaryl, and arylalkyl groups having 1 to 10 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 138A,
wherein R 9 is as defined above; and
(d) reacting the hydrohalide salt from step “c” with an organometallic compound capable of displacing X 2 of Formula 138A with a 3-fluorophenyl moiety of Formula B′,
to produce compound 116.
15. The process of claim 14 wherein the organometallic compound used in step “d” is selected from the group consisting of: fluoroaryl-alkylboranes; fluoroaryl-haloboranes; and fluoroaryl-zinc, -aluminium, -magnesium, and -tin reagents.