Synthesizing method for 4-amino-2-methyl-5-(brooethyl) pyrimidine hydrobromide

A technology of pyrimidine hydrobromide and synthesis method, which is applied in the field of synthesis of 4-amino-2-methyl-5-pyrimidine hydrobromide, can solve the problems of limited application, non-compliance with environmental protection requirements, cumbersome operation, etc. Achieve the effects of easy industrial scale production, green production method and low requirements for process equipment

Inactive Publication Date: 2017-11-24
CHENGDU BAISHIXING SCI & TECH IND
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  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

[0008] 4-Amino-2-methyl-5-cyanopyrimidine is an important intermediate in the modern synthesis of vitamin B1. It is expensive and there are relatively few domestic manufacturers
The above-mentioned method 1 and method 2 have lengthy process routes, complex reactions, low yields and high costs, which limit their application in production
[0009] Method 3: U.S. Patent US2016122319 discloses a simple method of directly hydrogenating and reducing 4-amino-2-methyl-5-cyanopyrimidine under pressure, which requires 20 kg of pressure to achieve, which also limits its Application in actual production
[0010] It can be seen that the above process scheme has many reaction steps, cumbersome operation, difficult separation and purification, high cost, and does not meet environmental protection requirements. Therefore, it is urgent to develop a short synthetic route, simple operation, low cost, and green environmental protection. A new method of 2-methyl-5-(bromomethyl)pyrimidine hydrobromide

Method used

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  • Synthesizing method for 4-amino-2-methyl-5-(brooethyl) pyrimidine hydrobromide
  • Synthesizing method for 4-amino-2-methyl-5-(brooethyl) pyrimidine hydrobromide
  • Synthesizing method for 4-amino-2-methyl-5-(brooethyl) pyrimidine hydrobromide

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Experimental program
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Effect test

Embodiment 1

[0032] Embodiment 1: a kind of synthetic method of 4-amino-2-methyl-5-(bromomethyl) pyrimidine hydrobromide, comprises the following steps:

[0033] S1.3-Methoxypropionitrile and ethyl formate were subjected to the action of sodium methoxide to obtain formylated intermediate sodium salt A; the solvent used was tetrahydrofuran, and the reaction temperature was 0°C;

[0034] S2. Intermediate sodium salt A reacts with dimethyl sulfate to obtain intermediate B; the solvent used is dichloromethane, and the reaction temperature is 0°C;

[0035] S3. Intermediate B and acetamidine hydrochloride are condensed to obtain intermediate C; the solvent used is ethanol, and the reaction temperature is 0°C;

[0036] S4. Intermediate C reacts with hydrobromic acid to obtain the target product 4-amino-2-methyl-5-(bromomethyl)pyrimidine hydrobromide I; the solvent used is acetic acid, and the reaction temperature is 0°C.

Embodiment 2

[0037] Embodiment 2: a kind of synthetic method of 4-amino-2-methyl-5-(bromomethyl) pyrimidine hydrobromide, comprises the following steps:

[0038] S1.3-Methoxypropionitrile and ethyl formate were subjected to the action of sodium methoxide to obtain formylated intermediate sodium salt A; the solvent used was methyl tetrahydrofuran, and the reaction temperature was 100°C;

[0039] S2. The intermediate sodium salt A is reacted with dimethyl sulfate to obtain the intermediate B; the solvent used is dichloroethane, and the reaction temperature is 100°C;

[0040] S3. Intermediate B and acetamidine hydrochloride are condensed to obtain intermediate C; the solvent used is methanol, and the reaction temperature is 100° C.;

[0041] S4. Intermediate C reacts with hydrobromic acid to obtain the target product 4-amino-2-methyl-5-(bromomethyl)pyrimidine hydrobromide I; the solvent used is formic acid, and the reaction temperature is 150°C.

Embodiment 3

[0042] Embodiment 3: a kind of synthetic method of 4-amino-2-methyl-5-(bromomethyl) pyrimidine hydrobromide, comprises the following steps:

[0043] S1.3-Methoxypropionitrile and ethyl formate are obtained under the action of sodium methoxide to obtain formylated intermediate sodium salt A; the solvent used is diethyl ether, and the reaction temperature is 10°C;

[0044] S2. Intermediate sodium salt A reacts with dimethyl sulfate to obtain intermediate B; the solvent used is chloroform, and the reaction temperature is 10°C;

[0045] S3. Intermediate B and acetamidine hydrochloride are condensed to obtain intermediate C; the solvent used is isopropanol, and the reaction temperature is 10° C.;

[0046] S4. Intermediate C reacts with hydrobromic acid to obtain the target product 4-amino-2-methyl-5-(bromomethyl)pyrimidine hydrobromide I; the solvent used is propionic acid, and the reaction temperature is 15°C.

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Abstract

The invention discloses a synthesizing method for 4-amino-2-methyl-5-(brooethyl) pyrimidine hydrobromide. The method comprises the following steps: acquiring formylated midbody sodium salt A by reacting 3-methoxypropionitrile with ethyl formate under the effect of sodium methylate; reacting the midbody sodium salt A with dimethyl sulfate, thereby acquiring a midbody B; condensing the midbody B with acetamidine hydrochloride, thereby acquiring a midbody C; and reacting the midbody C with hydrobromic acid, thereby acquiring a target product 4-amino-2-methyl-5-(brooethyl) pyrimidine hydrobromide I. According to the invention, the raw material source is wide and the cost is low; the synthesizing method is simple in production operation and has low requirement for processing equipment; the rigorous production conditions, such as, anhydrous condition, anaerobic condition and high-pressure hydrogenation, are not required; the reaction condition is mild; the method is easy for large-scale industrial production; the process is simple; the production period is short; the production efficiency is high; the production method is green and environmentally friendly and is suitable for large-scale industrial production.

Description

technical field [0001] The invention belongs to the field of organic chemistry, and in particular relates to a synthesis method of 4-amino-2-methyl-5-(bromomethyl)pyrimidine hydrobromide. Background technique [0002] 4-Amino-2-methyl-5-(bromomethyl)pyrimidine hydrobromide is an important pharmaceutical intermediate, which was first used in the total synthesis of vitamin B1, and can also be used as an important synthetic building block for other advanced drugs . Vitamin B1, also known as thiamine, was the first B vitamin to be identified. Thiamine-dependent enzyme acts as a cofactor for several enzymes involved in energy metabolism, which is important for the synthesis and production of neurotransmitters, substances used in the defense against oxidative stress reduction. Vitamin B1 mainly exists in the outer skin and germ of seeds, and the vitamin B1 currently used by people is the product of chemical synthesis. [0003] There are few reports on the synthesis of 4-amino-2...

Claims

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Application Information

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Patent Type & Authority Applications(China)
IPC IPC(8): C07D239/42
CPCC07D239/42
Inventor 石常青
Owner CHENGDU BAISHIXING SCI & TECH IND
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