IP Library Granted Patent US 11,453,648
Granted Patent B2
US 11,453,648 · App. 17/291,662 · Granted Sep 27, 2022

Method for producing orotic acid derivative

Inventors: Motoki Murai (Kawasaki, JP); Akira Shibuya (Kawasaki, JP)
Assignee: SHOWA DENKO K.K.
C07D239/557C07D239/545
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Quick Facts
Patent No.
US 11,453,648
App. No.
17/291,662
Granted
Sep 27, 2022
Kind
B2
Abstract

Provided is a method for producing an orotic acid derivative, the method comprising a condensation step of performing, under a basic condition, a condensation reaction between an orotic acid halide represented by General Formula (I) and a compound represented by General Formula (II) to generate an orotic acid derivative represented by General Formula (III); and a neutralization crystallization step of precipitating crystals of orotic acid by neutralization crystallization to separate a liquid containing the orotic acid derivative from the crystals of orotic acid, after the condensation step. In General Formula (I), (II), or (III), X is a halogen atom, and A is a group represented by General Formula (A-1) or (A-2). In General Formula (A-1) or (A-2), R 1 is a hydrogen atom or an organic group, and R 2 and R 3 are each independently an organic group. In a case where R 1 is an organic group, R 1 and R 2 may be bonded to each other to form a ring.

Claims (19)

1. A method for producing an orotic acid derivative, comprising:

performing, under a basic condition, a condensation reaction between an orotic acid halide represented by General Formula (I) and a compound represented by General Formula (II) to generate an orotic acid derivative represented by General Formula (III); and

precipitating crystals of orotic acid by neutralization crystallization to separate a liquid containing the orotic acid derivative from the crystals of orotic acid, after the condensation reaction,

wherein X is a halogen atom, and A is a group represented by General Formula (A-1) or (A-2);

wherein R 1 is a hydrogen atom or an organic group, and R 2 and R 3 are each independently an organic group, in a case where R 1 is an organic group, R 1 and R 2 may be bonded to each other to form a ring, and * is a bonding position at which the hydrogen atom in General Formula (II) is bonded.

2. The method for producing an orotic acid derivative according to claim 1 , wherein in General Formula (A-1), le is a hydrogen atom or an organic group having 1 to 10 carbon atoms, and R 2 is an organic group having a carboxy group and having 1 to 15 carbon atoms, and

in General Formula (A-2), R 3 is an organic group having 1 to 15 carbon atoms.

3. The method for producing an orotic acid derivative according to claim 1 , wherein the compound represented by General Formula (II) is an amino acid.

4. The method for producing an orotic acid derivative according to claim 3 , wherein the amino acid is glutamic acid.

5. The method for producing an orotic acid derivative according to claim 1 , to wherein a solvent used in the condensation reaction is a non-halogenic solvent.

6. The method for producing an orotic acid derivative according to claim 5 , wherein the solvent is a water-containing solvent.

7. The method for producing an orotic acid derivative according to claim 6 , wherein the solvent is a two-phase solvent of an organic solvent and water.

8. The method for producing an orotic acid derivative according to claim 7 , wherein the organic solvent is tetrahydrofuran or toluene.

9. The method for producing an orotic acid derivative according to claim 1 , wherein a pH of a liquid phase is set to 4 to 6 in the neutralization crystallization step.

10. The method for producing an orotic acid derivative according to claim 1 , further comprising subjecting the liquid containing the orotic acid derivative to secondary neutralization crystallization to precipitate crystals of the orotic acid derivative, after the neutralization crystallization.

11. The method for producing an orotic acid derivative according to claim 10 , wherein a pH of a liquid phase is set to 0.5 to 2 in the secondary neutralization crystallization.

12. The method for producing an orotic acid derivative according to claim 10 , further comprising collecting the crystals of the orotic acid derivative, after the secondary neutralization crystallization.

13. The method for producing an orotic acid derivative according to claim 1 , further comprising reacting an orotic acid with a thionyl halide to generate the orotic acid halide, before the condensation reaction.

14. The method for producing an orotic acid derivative according to claim 1 , wherein the orotic acid halide is orotic acid chloride.

Assignments (3)
CHANGE OF ADDRESS Recorded Feb 14, 2024
From: RESONAC CORPORATION
To: RESONAC CORPORATION
Reel/Frame 066599/0037 →
CHANGE OF NAME Recorded Jun 23, 2023
From: SHOWA DENKO K.K.
To: RESONAC CORPORATION
Reel/Frame 064082/0513 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded May 6, 2021
From: MURAI, MOTOKI; SHIBUYA, AKIRA
To: SHOWA DENKO K.K.
Reel/Frame 056158/0701 →
Priority Claims (1)
JP JP2018-212455 · Nov 12, 2018 · national
Continuity (1)
Related Publication 20220002253A1 · Jan 6, 2022