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HRID 620261作成日:2026年10月24日

Methane → Metoclopramide sulfide

https://huagongshe.com/ja/reaction/620261

反応式

関与物質

役割名称HCID仕込み量
反応物MethaneHCID 297—
反応物Sodium IodideHCID 5238—
反応物2-Chloroethyl methyl sulfideHCID 10965—
反応物Potassium CarbonateHCID 11430—
反応物4-amino-5-chloro-N-(2-(diethylamino)ethyl)-2-hydroxybenzamide hydrochlorideHCID 14116877—
溶媒DimethylformamideHCID 6228—
溶媒AcetonitrileHCID 6342—
生成物Metoclopramide sulfideHCID 12409832%

反応手順

A stirred mixture of 4-amino-5-chloro-N-[2-(diethylamino)ethyl]-2-hydroxybenzamide hydrochloride (10.0 g, 31.06 mmoles) (from Preparation No. 1A), anhydrous potassium carbonate (12.84 g, 93.16 mmoles), sodium iodide (4.66 g, 31.06 mmoles) and 2-chloroethyl methyl sulfide (3.70 ml, 4.10 g, 37.26 mmoles) in 60 ml dry DMF was refluxed for 10 hours. The solvent was evaporated under reduced pressure and the dark semi-solid was partitioned between water and methylene chloride. Sodium hydroxide solution was added to bring the pH of the aqueous layer to 14. The mixture was shaken well and the layers were separated. The aqueous layer was extracted with 3 portions of methylene chloride. The combined organic solutions were dried over MgSO4 and evaporated. The solid obtained was dissolved in 100 ml of warm acetonitrile. The solution was treated with Darco G-60, filtered, evaporated to 30 ml, and stored at -15°. The solid was filtered to give 3.56 g (32%) of the title compound as off-white crystals, mp. 118°-120°.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US04820715
出典データセットuspto-grants-1989_04
ORD IDord-c2297b3ed368483eb86bef2004703dbf
出典メモuspto-grants-1989_04