Bis-phosphate compound and asymmetric reaction using the same
View Patent ↗A novel bis-phosphate compound is provided which can be applied to a wide range of reactive substrates and reactions as an asymmetric reaction catalyst and can realize an asymmetric reaction affording a high yield and a high enantiomeric excess. The bis-phosphate compound has a tetraaryl skeleton represented by General Formula (1). In an asymmetric reaction, an amidodiene and an unsaturated aldehyde compound are reacted with each other in the presence of the optically active bis-phosphate compound to give an optically active amidoaldehyde. The invention allows a reaction such as an asymmetric Diels-Alder reaction to proceed efficiently, which has been difficult with conventional mono-phosphate compounds. Thus, the invention enables an industrially feasible method for the production of optically active amidoaldehydes, optically active β-amino acid derivatives, optically active diamine compounds, optically active pyrrolidine derivatives and optically active dihydropyran derivatives which are useful as products such as medicines, agricultural chemicals and chemical products as well as synthesis intermediates for such products.
1. A bis-phosphate compound comprising a tetraaryl skeleton of formula (1):
wherein:
R 1 to R 14 are each independently a hydrogen atom, an optionally substituted hydrocarbon group, an optionally substituted heterocyclic group, a hydroxyl group, an optionally substituted alkoxy group, an optionally substituted aryloxy group, an optionally substituted acyl group, an optionally substituted alkoxycarbonyl group, an optionally substituted aryloxycarbonyl group, an optionally substituted carbamoyl group, an optionally substituted alkylthiocarbonyl group, an optionally substituted arylthiocarbonyl group, a carboxyl group, an optionally substituted alkylthio group, an optionally substituted arylthio group, an optionally substituted amino group, a substituted silyl group, or a halogen atom; in any combination of R 1 to R 14 , these substituents may be linked together to form a ring;
X 1 to X 14 are each independently a carbon atom or a nitrogen atom, wherein in the case of a nitrogen atom, there is no substituent on the nitrogen atom;
A 1 to A 6 are each independently an oxygen atom or a sulfur atom; and
the —OH group in the phosphate moiety may form a metal salt, an ammonium salt, or an amine salt.
2. The bis-phosphate compound of claim 1 , wherein the bis-phosphate compound is optically active.
3. The bis-phosphate compound of claim 2 , wherein the bis-phosphate compound is optically active due to axial chirality.
4. A process, comprising:
performing an asymmetric reaction in the presence of an optically active bis-phosphate compound of claim 2 .
5. The process of claim 4 , wherein an amidodiene and an unsaturated aldehyde compound are reacted with each other in the presence of the optically active bis-phosphate compound, to produce an optically active amidoaldehyde.
6. The process of claim 4 , wherein an imine and a 1,3-diketone are reacted with each other in the presence of the optically active bis-phosphate compound, to produce an optically active β-aminoketone.
7. The process of claim 4 , wherein an imine and a furan are reacted with each other in the presence of the optically active bis-phosphate compound, to produce an optically active furanylamine.
8. The process of claim 4 , wherein an imine and a carbamate are reacted with each other in the presence of the optically active bis-phosphate compound, to produce an optically active β-aminoketone.
9. A method for producing a bis-phosphate compound of claim 1 , the method comprising:
reacting a compound of formula (N) with a phosphorylating agent:
wherein:
R 1 to R 14 are each independently a hydrogen atom, an optionally substituted hydrocarbon group, an optionally substituted heterocyclic group, a hydroxyl group, an optionally substituted alkoxy group, an optionally substituted aryloxy group, an optionally substituted acyl group, an optionally substituted alkoxycarbonyl group, an optionally substituted aryloxycarbonyl group, an optionally substituted carbamoyl group, an optionally substituted alkylthiocarbonyl group, an optionally substituted arylthiocarbonyl group, a carboxyl group, an optionally substituted alkylthio group, an optionally substituted arylthio group, an optionally substituted amino group, a substituted silyl group or a halogen atom; in any combination of R 1 to R 14 , these substituents may be linked together to form a ring;
X 1 to X 14 are each independently a carbon atom or a nitrogen atom, wherein in the case of a nitrogen atom, there is no substituent on the nitrogen atom; and
A 1 to A 4 are each independently an oxygen atom or a sulfur atom.
10. The method of claim 9 , wherein the phosphorylating agent is at least one selected from the group consisting of a phosphorus oxyhalide, a phosphorus halide, a dihalogenophosphine, and a thiophosphoryl halide.
11. A process, comprising:
performing an asymmetric reaction in the presence of an optically active bis-phosphate compound of claim 3 .
12. The process of claim 11 , wherein an amidodiene and an unsaturated aldehyde compound are reacted with each other in the presence of the optically active bis-phosphate compound, to produce an optically active amidoaldehyde.
13. The process of claim 11 , wherein an imine and a 1,3-diketone are reacted with each other in the presence of the optically active bis-phosphate compound, to produce an optically active β-aminoketone.
14. The process of claim 11 , wherein an imine and a furan are reacted with each other in the presence of the optically active bis-phosphate compound, to produce an optically active furanylamine.
15. The process of claim 11 , wherein an imine and a carbamate are reacted with each other in the presence of the optically active bis-phosphate compound, to produce an optically active β-aminoketone.
16. The method of claim 9 , wherein the phosphorylating agent is a phosphorus oxyhalide.
17. The method of claim 9 , wherein the phosphorylating agent is a phosphorus halide.
18. The method of claim 9 , wherein the phosphorylating agent is a dihalogenophosphine.
19. The method of claim 9 , wherein the phosphorylating agent is a thiophosphoryl halide.