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HRID 652034作成日:2026年10月27日

Methanesulfonamide → N-[4-[14-(Trimethylsilyl)tetradecylamino]benzoyl]methanesulfonamide

https://huagongshe.com/reaction/652034

反応式

関与物質

役割名称HCID仕込み量
反応物MethanesulfonamideHCID 72879—
反応物4-[14-(Trimethylsilyl)tetradecylamino]benzoyl chloride hydrochlorideHCID 20198230—
溶媒PyridineHCID 1049—
生成物N-[4-[14-(Trimethylsilyl)tetradecylamino]benzoyl]methanesulfonamideHCID 20198291—

反応手順

A solution of 12.3 g. of 4-[14-(trimethylsilyl)tetradecylamino]benzoyl chloride hydrochloride and 2.8 g. of methanesulfonamide in 150 ml. of pyridine is stirred at reflux for 2 hours and then evaporated in vacuo. The residue is partitioned between water and diethyl ether, the aqueous layer acidified with 1N hydrochloric acid, and the organic layer separated, dried with magnesium sulfate and evaporated. Crystallization of the residue affords the product as a white solid.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US04670421
出典データセットuspto-grants-1987_06
ORD IDord-ae62468ef3c546e7b5459000a2be9856
出典メモuspto-grants-1987_06