Process for producing optically active beta-hydroxy-alpha-aminocarboxylic acid ester

1. A process for producing an optically active β-hydroxy-α-aminocarboxylic acid ester;

comprising a step of asymmetric reduction reaction of a β-keto-α-aminocarboxylic acid ester represented by the general formula (2):

wherein, R 4 is a hydrogen atom, an optionally substituted alkyl group having 1 to 21 carbon atoms, an optionally substituted alkenyl group having 2 to 21 carbon atoms, an optionally substituted alkynyl group having 2 to 21 carbon atoms, or an optionally substituted aralkyl group having 7 to 20 carbon atoms; R 5 is an optionally substituted alkyl group having 1 to 10 carbon atoms, an optionally substituted aralkyl group having 7 to 20 carbon atoms, or an optionally substituted aryl group having 6 to 20 carbon atoms; R 6 and R 7 each may be the same or different, and is a hydrogen atom, an optionally substituted alkyl group having 1 to 10 carbon atoms, an optionally substituted aralkyl group having 7 to 20 carbon atoms, an optionally substituted aryl group having 6 to 20 carbon atoms, an optionally substituted acyl group having 1 to 40 carbon atoms, or an amino-protecting group; R 6 and R 7 may constitute a heterocycle together with the neighboring nitrogen atom,

in the presence of an optically active amine complex represented by the general formula (1):

wherein, * indicates an asymmetric carbon atom; R 1 and R 2 each may be the same or different, and is an optionally substituted alkyl group having 1 to 21 carbon atoms, an optionally substituted aralkyl group having 7 to 20 carbon atoms, or an optionally substituted aryl group having 6 to 20 carbon atoms; further, R 1 and R 2 may constitute a ring; R 3 is a hydrogen atom, an optionally substituted alkyl group having 1 to 21 carbon atoms, an optionally substituted aralkyl group having 7 to 20 carbon atoms, or an optionally substituted aryl group having 6 to 20 carbon; Ar is an optionally substituted aromatic compound; M is a transition metal; Z is a halogen atom, an optionally substituted alkylsulfonyloxy group, an optionally substituted arylsulfonyloxy group, or an optionally substituted aralkylsulfonyloxy group; and Y is an oxygen atom, or ═N—S(O 2 )—R wherein R is an optionally substituted alkyl group, an optionally substituted aryl group or an optionally substituted aralkyl group,

and hydrogen or a hydrogen donor compound;

wherein, the optically active β-hydroxy-α-aminocarboxylic acid ester is represented by the following general formula (3) or general formula (4):

wherein, * indicates an asymmetric carbon atom unless R 4 is a hydrogen atom; R 4 , R 5 , R 6 and R 7 are the same as described above.

2. The production process according to claim 1 , wherein formic acid is used as the hydrogen donor compound.

3. The production process according to claim 1 , wherein the reaction is carried out in the presence of a base.

4. A process for producing a β-keto-α-aminocarboxylic acid ester;

comprising a step of reacting a glycine derivative represented by the general formula (5):

wherein, R 5 is an optionally substituted alkyl group having 1 to 10 carbon atoms, an optionally substituted aralkyl group having 7 to 20 carbon atoms, or an optionally substituted aryl group having 6 to 20 carbon atoms; R 6 and R 7 each may be the same or different, and is a hydrogen atom, an optionally substituted alkyl group having 1 to 10 carbon atoms, an optionally substituted aralkyl group having 7 to 20 carbon atoms, an optionally substituted aryl group having 6 to 20 carbon atoms, an optionally substituted acyl group having 1 to 40 carbon atoms, or an amino-protecting group; and R 6 and R 7 may constitute a heterocycle together with the neighboring nitrogen atom,

with a carboxylic acid derivative represented by the general formula (6):

wherein, X is a halogen atom, an optionally substituted acyloxy group, an optionally substituted alkyloxycarbonyloxy group, an optionally substituted sulfonyloxy group, an optionally substituted alkyloxy group, an optionally substituted aryloxy group, or an optionally substituted imidazole group; and R 4 is hydrogen atom, an optionally substituted alkyl group having 1 to 21 carbon atoms, an optionally substituted alkenyl group having 2 to 21 carbon atoms, an optionally substituted alkynyl group having 2 to 21 carbon atoms, an optionally substituted aralkyl group having 7 to 20 carbon atoms, or an optionally substituted aryl group having 6 to 20 carbon atoms,

in the presence of a Lewis acid and an amine;

wherein the β-keto-α-aminocarboxylic acid ester is represented by the general formula (2):

wherein, R 4 , R 5 , R 6 and R 7 are the same as described above.

5. The production process according to claim 4 , wherein the Lewis acid is titanium tetrachloride.

6. The production process according to claim 4 , wherein R 4 is an optionally substituted alkyl group having 11 to 21 carbon atoms, an optionally substituted alkenyl group having 11 to 21 carbon atoms, or an optionally substituted alkynyl group having 11 to 21 carbon atoms.

7. The production process according to claim 4 , wherein the reaction is carried out at −40° C. or higher.

8. A process for producing an optically active β-hydroxy-α-aminocarboxylic acid ester;

comprising a step of asymmetric hydrogenation reaction of a β-keto-α-aminocarboxylic acid ester using a transition metal complex having an optically active phosphine ligand as a catalyst;

and a step of inverting the steric configuration of the hydroxyl group at the 3-position, if necessary;

wherein the optically active β-hydroxy-α-aminocarboxylic acid ester is represented by the general formula (3) or (4):

wherein, * indicates an asymmetric carbon atom unless R 4 is a hydrogen atom; R 4 is a hydrogen atom, an optionally substituted alkyl group having 1 to 21 carbon atoms, an optionally substituted alkenyl group having 2 to 21 carbon atoms, an optionally substituted alkynyl group having 2 to 21 carbon atoms, an optionally substituted aralkyl group having 7 to 20 carbon atoms, or an optionally substituted aryl group having 6 to 20 carbon atoms; R 5 is an optionally substituted alkyl group having 1 to 10 carbon atoms, an optionally substituted aralkyl group having 7 to 20 carbon atoms, or an optionally substituted aryl group having 6 to 20 carbon atoms; R 6 and R 7 each may be the same or different, and is a hydrogen atom, an optionally substituted alkyl group having 1 to 10 carbon atoms, an optionally substituted aralkyl group having 7 to 20 carbon atoms, an optionally substituted aryl group having 6 to 20 carbon atoms, an optionally substituted acyl group having 1 to 40 carbon atoms, or an amino-protecting group; R 6 and R 7 may constitute a heterocycle together with the neighboring nitrogen atom, and

wherein the β-keto-α-aminocarboxylic acid ester is represented by the general formula (2):

wherein, R 4 , R 5 , R 6 and R 7 are the same as described above, and is produced by a process comprising a step of reacting a glycine derivative represented by the general formula (5):

wherein, R 5 , R 6 and R 7 are the same as described above,

with a carboxylic acid derivative represented by the general formula (6):

wherein, X is a halogen atom, an optionally substituted acyloxy group, an optionally substituted alkyloxycarbonyloxy group, an optionally substituted sulfonyloxy group, an optionally substituted alkyloxy group, an optionally substituted aryloxy group, or an optionally substituted imidazole group; and R 4 is the same as described above,

in the presence of a Lewis acid and an amine.

9. A process for producing an optically active β-hydroxy-α-aminocarboxylic acid ester comprising a step of asymmetric reduction reaction of a β-keto-α-aminocarboxylic acid ester in the presence of an optically active amine complex and hydrogen or a hydrogen donor compound,

wherein:

the optically activeβ-hydroxy-α-aminocarboxylic acid ester is represented by the following general formula (3) or general formula (4):

wherein, * indicates an asymmetric carbon atom unless R 4 is a hydrogen atom; R 4 is a hydrogen atom, an optionally substituted alkyl group having 1 to 21 carbon atoms, an optionally substituted alkenyl group having 2 to 21 carbon atoms, an optionally substituted alkenyl group having 2 to 21 carbon atoms, or an optionally substituted aralkyl group having 7 to 20 carbon atoms; R 5 is an optionally substituted alkyl group having 1 to 10 carbon atoms, an optionally substituted aralkyl group having 7 to 20 carbon atoms, or an optionally substituted aryl group having 6 to 20 carbon atoms; R 6 and R 7 each may be the same or different, and is a hydrogen atom, an optionally substituted alkyl group having 1 to 10 carbon atoms, an optionally substituted aralkyl group having 7 to 20 carbon atoms, an optionally substituted aryl group having 6 to 20 carbon atoms, an optionally substituted acyl group having 1 to 40 carbon atoms, or an amino-protecting group; R 6 and R 7 may constitute a heterocycle together with the neighboring nitrogen atom,

the β-keto-α-aminocarboxylic acid ester is represented by the general formula (2):

wherein R 4 , R 5 , R 6 and R 7 are the same as described above,

and is obtained by a process comprising a step of reacting a glycine derivative represented by the general formula (5):

wherein, R 5 , R 6 and R 7 are the same as described above,

with a carboxylic acid derivative represented by the general formula (6):

wherein, X is a halogen atom, an optionally substituted acyloxy group, an optionally substituted alkyloxycarbonyloxy group, an optionally substituted sulfonyloxy group, an optionally substituted alkyloxy group, an optionally substituted aryloxy group, or an optionally substituted imidazole group; and R 4 is the same as described above,

in the presence of a Lewis acid and an amine, and

the optically active amine complex is represented by the general formula (1):

wherein, * indicates an asymmetric carbon atom; R 1 and R 2 each may be the same or different, and is an optionally substituted alkyl group having 1 to 21 carbon atoms, an optionally substituted aralkyl group having 7 to 20 carbon atoms, or an optionally substituted aryl group having 6 to 20 carbon atoms; further, R 1 and R 2 may constitute a ring; R 3 is a hydrogen atom, an optionally substituted alkyl group having 1 to 21 carbon atoms, an optionally substituted aralkyl group having 7 to 20 carbon atoms, or an optionally substituted aryl group having 6 to 20 carbon; Ar is an optionally substituted aromatic compound; M is a transition metal; Z is a halogen atom, an optionally substituted alkylsulfonyloxy group, an optionally substituted arylsulfonyloxy group, or an optionally substituted aralkylsulfonyloxy group; and Y is an oxygen atom, or ═N—S(O 2 )—R wherein R is an optionally substituted alkyl group, an optionally substituted aryl group or an optionally substituted aralkyl group.

10. A process for producing an optically active 2-amino-1,3-diol derivative;

comprising a step of reducing the ester part of an optically active β-hydroxy-α-aminocarboxylic acid ester;

and a step of converting the substituent group at the amino group into an acyl group if necessary;

wherein the optically active 2-amino-1,3-diol derivative is represented by the general formula (7) or general formula (8):

wherein, * indicates an asymmetric carbon atom unless R 4 is a hydrogen atom; R 4 is a hydrogen atom, an optionally substituted alkyl group having 1 to 21 carbon atoms, an optionally substituted alkenyl group having 2 to 21 carbon atoms, an optionally substituted alkynyl group having 2 to 21 carbon atoms, or an optionally substituted aralkyl group having 7 to 20 carbon atoms; and R 8 is an optionally substituted alkyl group or an alkanoyl group, having 11 to 40 carbon atoms, and

wherein the optically active β-hydroxy-α-aminocarboxylic acid ester is produced by a process comprising a step of asymmetric reduction reaction of a β-keto-α-aminocarboxylic acid ester represented by the general formula (2):

wherein, R 4 is the same as described above; R 5 is an optionally substituted alkyl group having 1 to 10 carbon atoms, an optionally substituted aralkyl group having 7 to 20 carbon atoms, or an optionally substituted aryl group having 6 to 20 carbon atoms; R 6 and R 7 each may be the same or different, and is a hydrogen atom, an optionally substituted alkyl group having 1 to 10 carbon atoms, an optionally substituted aralkyl group having 7 to 20 carbon atoms, an optionally substituted aryl group having 6 to 20 carbon atoms, an optionally substituted acyl group having 1 to 40 carbon atoms, or an amino-protecting group; R 6 and R 7 may constitute a heterocycle together with the neighboring nitrogen atom,

in the presence of an optically active amine complex represented by the general formula (1):

wherein, * indicates an asymmetric carbon atom; R 1 and R 2 each may be the same or different, and is an optionally substituted alkyl group having 1 to 21 carbon atoms, an optionally substituted aralkyl group having 7 to 20 carbon atoms, or an optionally substituted aryl group having 6 to 20 carbon atoms; further, R 1 and R 2 may constitute a ring; R 3 is a hydrogen atom, an optionally substituted alkyl group having 1 to 21 carbon atoms, an optionally substituted aralkyl group having 7 to 20 carbon atoms, or an optionally substituted aryl group having 6 to 20 carbon; Ar is an optionally substituted aromatic compound; M is a transition metal; Z is a halogen atom, an optionally substituted alkylsulfonyloxy group, an optionally substituted arylsulfonyloxy group, or an optionally substituted aralkylsulfonyloxy group; and Y is an oxygen atom, or ═N—S(O 2 )—R wherein R is an optionally substituted alkyl group, an optionally substituted aryl group or an optionally substituted aralkyl group,

and hydrogen or a hydrogen donor compound, and

the optically active β-hydroxy-α-aminocarboxylic acid ester is represented by the following general formula (3) or general formula (4):

wherein, * indicates an asymmetric carbon atom unless R 4 is a hydrogen atom; R 4 , R 5 , R 6 and R 7 are the same as described above.

11. The production process according to claim 10 , wherein a reducing agent for reducing the ester part is sodium borohydride.

12. The production process according to claim 11 , wherein the reduction is carried out in the presence of a Lewis acid.

13. The production process according to claim 12 , wherein the Lewis acid is calcium chloride.

14. The production process according to claim 1 , wherein the optically active β-hydroxy-α-aminocarboxylic acid ester is in anti-form.

15. The production process according to claim 9 , wherein the optically active β-hydroxy-α-aminocarboxylic acid ester is in anti-form.