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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 620261생성일: 2026년 10월 24일

Methane → Metoclopramide sulfide

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

반응식

참여 물질

역할이름HCID투입량
반응물MethaneHCID 297—
반응물Sodium IodideHCID 5238—
반응물2-Chloroethyl methyl sulfideHCID 10965—
반응물Potassium CarbonateHCID 11430—
반응물4-amino-5-chloro-N-(2-(diethylamino)ethyl)-2-hydroxybenzamide hydrochlorideHCID 14116877—
용매DimethylformamideHCID 6228—
용매AcetonitrileHCID 6342—
생성물Metoclopramide sulfideHCID 12409832%

반응 단계

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°.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04820715
출처 데이터셋uspto-grants-1989_04
ORD IDord-c2297b3ed368483eb86bef2004703dbf
출처 메모uspto-grants-1989_04