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HRID 7199作成日:2026年10月23日

Methyl Bromide → p-Toluenesulfonic acid

https://huagongshe.com/ja/reaction/7199

反応式

関与物質

役割名称HCID仕込み量
反応物Methyl BromideHCID 6323—
反応物Methyl ChlorideHCID 6327—
反応物Methyl iodideHCID 6328—
反応物Methyl p-toluenesulfonateHCID 6645—
反応物TetramethylureaHCID 12437—
溶媒AcetoneHCID 180—
溶媒IsopropanolHCID 3776—
溶媒DimethylformamideHCID 6228—
溶媒TetrahydrofuranHCID 8028—
生成物p-Toluenesulfonic acidHCID 6101—

反応手順

The methylation of the pyridine nitrogen atom in the compound of the formula XXIII, with formation of the pyridinium salt of the formula XXIV, can be carried out smoothly with numerous methylating agents, for example methyl iodide, methyl bromide, methyl chloride or methyl toluene-4-sulfonate, in a number of solvents, for example alcohols, such as isopropanol, amides, such as DMF, N,N,N′,N′-tetramethylurea, ketones, such as acetone, or ethers, such as THF, preferably at temperatures of from about 40 to about 60° C. In the reaction of the compound of the formula XXIII with methyl chloride in DMF at 45° C., for example, the compound of the formula XXIV where X=Cl is obtained in quantitative yield and a purity of about 98.4%. When the methylation is carried out on an industrial scale, it is preferred to use a less volatile methylating agent. Since an additional anion exchange, for example by ion exchange chromatography, is to be avoided if possible, a further aspect in the selection of the methylating agent is the effect of the anion X, contained in the compounds of the formulae IV, IX and I and originating from the methylating agent, on the properties of these compounds, for example on the solubility of the compound of the formula IV or a salt thereof, which is of importance in the coupling reaction of the compounds of the formulae III and IV, or on the solubilities, the precipitation properties and the physiological compatibility of the compound of the formula I. Overall, the iodides and toluene-4-sulfonates have, based on their properties, been found to be particularly favorable, preferred methylating agents thus being methyl iodide and methyl toluene-4-sulfonate (=methyl tosylate). The toluene-4-sulfonates, in particular, are distinguished, in the case of the compound of the formula IV or the toluene-4-sulfonic acid salt thereof, by the fact that they can be isolated easily, are highly soluble and have a high peptide coupling rate, and in the case of the compound of the formula I, in particular by surprisingly good precipitation properties, purity and yield. A particularly preferred methylating agent for the conversion of the compound of the formula XXIII into the compound of the formula XXIV thus is methyl toluene-4-sulfonate.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07084250B2
出典データセットuspto-grants-2006_08
ORD IDord-469d866e91794e08b6b711bc622a4f31
出典メモuspto-grants-2006_08