Concise β
The present invention provides a method for the synthesis of β 2 -amino acids. The method also provides methods yielding α-substituted β-amino aldehydes and β-substituted γ-amino alcohols. The present method according to this invention allows for increased yield and easier purification using minimal chromatography or crystallization. The methods described herein are based on an aldehyde aminomethylation which involves a Mannich reaction between an aldehyde and a formaldehyde-derived N,O-acetal (iminium precursor) and a catalyst, such as, for example, L-proline or a pyrrolidine. The invention allows for large scale, commercial preparation of β 2 -amino acids.
1. A method of synthesizing a β 2 amino acid by aldehyde aminomethylation, comprising steps of:
(a) reacting an aldehyde with an iminium ion via a Mannich reaction to yield an α-substituted β-amino aldehyde;
(b) reducing the α-substituted β-amino aldehyde in situ to a corresponding β-substituted γ-amino alcohol; and
(c) oxidizing the β-substituted γ-amino alcohol to provide a corresponding β 2 amino acid.
2. The method of claim 1 , wherein the method is stereoselective in the synthesis of the β 2 amino acid.
3. The method of claim 1 , wherein the method is diastereoselective in the synthesis of the β 2 amino acid.
4. The method of claim 1 , wherein the method is enantioselective in the synthesis of the β 2 amino acid.
5. The method of claim 1 , wherein the method yields a racemic mixture of the β 2 amino acid.
6. The method of claim 1 , wherein the method includes an additional step of protecting the corresponding β-substituted γ-amino alcohol to provide a protected β-substituted γ-amino alcohol that is then oxidized in step (c) to the corresponding β 2 amino acid in protected form.
7. The method of claim 1 wherein said iminium ion is chiral.
8. The method of claim 1 , wherein the Mannich reaction takes place in the presence of L-proline, L-alpha-m-proline, L-Pro-NH 2 , L-Pro-NHMe, L-Pro-NMe 2 , L-Pro-OMe, or a pyrrolidine catalyst.
9. The method of claim 1 , wherein the aldehyde has the structure
wherein R is Et, Pr, i-Pr, Bn, MeO 2 CCH 2 , n-Hex, CH 2 -iPr, CH 2 C 6 H 12 , (CH 2 ) 4 NHBoc, (Boc) 2 N(CH 2 ) 3 , MeO 2 CCH 2 ,
10. The method of claim 1 , wherein the iminium ion is generated in situ from a formaldehyde derived N,O-acetal having the structure:
11. A method of synthesizing a β-substituted γ-amino alcohol by aldehyde aminomethylation, comprising steps of:
(a) reacting an aldehyde with an iminium ion via a Mannich reaction to yield an α-substituted β-amino aldehyde; and
(b) reducing the α-substituted β-amino aldehyde in situ to a corresponding β-substituted γ-amino alcohol.
12. The method of claim 11 , wherein the method is stereoselective in the synthesis of the β-substituted γ-amino alcohol.
13. The method of claim 11 , wherein the method is diastereoselective in the synthesis of the β-substituted γ-amino alcohol.
14. The method of claim 11 , wherein the method is enantioselective in the synthesis of the β-substituted γ-amino alcohol.
15. The method of claim 11 , wherein the method yields a racemic mixture of the β-substituted γ-amino alcohol.
16. The method of claim 11 , wherein the method includes an additional step of protecting the corresponding β-substituted γ-amino alcohol to provide said β-substituted γ-amino alcohol in protected form.
17. The method of claim 11 , wherein said iminium ion is chiral.
18. The method of claim 11 , wherein the Mannich reaction takes place in the presence of L-proline, L-alpha-m-proline, L-Pro-NH 2 , L-Pro-NHMe, L-Pro-NMe 2 , L-Pro-OMe, or a pyrrolidine catalyst.
19. The method of claim 11 , wherein the aldehyde has the structure
wherein R is Et, Pr, i-Pr, Bn, MeO 2 CCH 2 , n-Hex, Ch 2 -iPr, CH 2 C 6 H 12 , (CH 2 ) 4 NHBoc,
20. The method of claim 11 , wherein the iminium ion is generated in situ from a formaldehyde derived N,O-acetal having the structure: