Synthesis method of 7- benzyloxy-6-methoxyl-4-hydroxyquinoline

A technology of hydroxyquinoline and synthetic method, applied in the direction of organic chemistry, etc., can solve problems such as unsuitable for industrial production, harsh reaction conditions, complicated post-processing, etc., and achieve the effect of avoiding column separation process, high conversion rate, and low cost

Active Publication Date: 2011-04-27
SHANGHAI CHEMPARTNER CO LTD
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  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

[0007] The technical problem to be solved by the present invention is to overcome the harsh reaction conditions, complicated post-treatment, high cost, many steps and complicated operation in the existing method for synthesizing 7-benzyloxy-6-methoxy-4-hydroxyquinoline , high risk, low yield, unsuitable for industrialized production and other defects, provides a simple and feasible, low cost, high yield, simple post-processing, safe and suitable for industrialized production of 7-benzyloxy-6-methanol The synthetic method of oxy-4-hydroxyquinoline

Method used

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  • Synthesis method of 7- benzyloxy-6-methoxyl-4-hydroxyquinoline
  • Synthesis method of 7- benzyloxy-6-methoxyl-4-hydroxyquinoline
  • Synthesis method of 7- benzyloxy-6-methoxyl-4-hydroxyquinoline

Examples

Experimental program
Comparison scheme
Effect test

Embodiment 1

[0048] Example 1 Preparation of 4-benzyloxy-5-methoxy-2-nitroacetophenone (compound B)

[0049] Compound A (67 g, 0.25 mol) was dissolved in dichloromethane (450 ml), cooled to -5°C with stirring. After 65% nitric acid (24 g, 0.25 mol, 17 ml) was dissolved in acetic acid (250 ml), it was added dropwise to the acetic anhydride solution of compound A, stirred at 0-5° C. for 20 hours, and the reaction was detected by LCMS to be complete.

[0050] After concentrating under reduced pressure to remove dichloromethane, the reaction solution was poured into stirred ice water, the precipitated solid was filtered, washed with water and beaten with absolute ethanol, and the solid was filtered and dried to obtain compound B, 62.8 g, yield 81%, liquid chromatography The detection purity is 96%.

Embodiment 2

[0051] Example 2 Preparation of 4-benzyloxy-5-methoxy-2-nitroacetophenone (compound B)

[0052] Compound A (67 g, 0.25 mol) was dissolved in acetic anhydride (450 ml), cooled to -5°C with stirring. After 65% nitric acid (44.9 g, 0.46 mol, 32 ml) was dissolved in acetic acid (450 ml), it was added dropwise to the acetic anhydride solution of compound A, stirred at 0-5° C. for 18 hours, and the reaction was detected by LCMS to be complete.

[0053] The reaction solution was poured into stirred ice water, and the precipitated solid was filtered, washed with water, slurried with absolute ethanol, and the solid was filtered and dried to obtain Compound B, 64.4 g, with a yield of 83% and a purity of 98% by liquid chromatography.

Embodiment 3

[0054] Example 3 Preparation of 4-benzyloxy-5-methoxy-2-nitroacetophenone (compound B)

[0055] Compound A (67 g, 0.25 mol) was dissolved in acetic anhydride (450 ml), cooled to -5°C with stirring. After 65% nitric acid (44.9 g, 0.46 mol, 32 ml) was dissolved in 96% sulfuric acid (240 ml), it was added dropwise in the acetic anhydride solution of compound A, stirred at 0-5° C. for 18 hours, and LCMS detected that the reaction was complete.

[0056] The reaction solution was poured into stirred ice water, the precipitated solid was filtered, washed with water, beaten with anhydrous 95% ethanol, and the solid was filtered and dried to obtain compound B, 66.0 g, yield 85%, purity 96% by liquid chromatography.

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Abstract

The invention discloses a synthesis method of 7-benzyloxy-6-methoxyl-4-hydroxyquinoline, which is characterized by comprising the following step of: under the action of proton acid, performing nitro reduction reaction and cyclization reaction for a compound C and a reducing agent to obtain a compound D, namely 7-benzyloxy-6-methoxyl-4-hydroxyquinoline. The synthesis method has the advantages of simple operation, mild reaction condition, high safety, high reactions conversion rate and selectivity, low cost and good environmental-protection property and conforms to the green chemistry standard of atom economy. By adopting post-processing methods, such as filtering, crystallizing and the like, the synthesis method is simple, convenient and feasible, and is suitable for both small-scale preparation in a laboratory and large-scale industrialized production.

Description

technical field [0001] The invention relates to a synthesis method of a pharmaceutical intermediate, in particular to a synthesis method of 7-benzyloxy-6-methoxy-4-hydroxyquinoline. Background technique [0002] 7-benzyloxy-6-methoxy-4-hydroxyquinoline (compound D), has the following structure: [0003] [0004] Wherein, Bn is benzyl. [0005] The compound is a quinoline compound, which is a commonly used intermediate in the field of pharmaceutical synthesis, and is especially widely used in the preparation of antimalarial drugs, antitumor drugs, anti-inflammatory and analgesic drugs, and the like. [0006] At present, the synthesis method of the compound D (US6809097B1) needs to adopt high-temperature heating to close the ring and separate the product through silica gel column. This method has the characteristics of high cost, complicated operation, large solvent requirement and high risk, and is not suitable for industrial production; The synthesis method of compound ...

Claims

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Application Information

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Patent Type & Authority Applications(China)
IPC IPC(8): C07D215/22
Inventor 何成江张贺王传旺
Owner SHANGHAI CHEMPARTNER CO LTD
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