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HRID 2394325作成日:2026年10月26日

Water → N1-[2-(4-cyanophenoxy)-1-methylethyl]-N2-phenoxycarbonyl-L-valinamide

https://huagongshe.com/reaction/2394325

反応式

関与物質

役割名称HCID仕込み量
反応物WaterHCID 962—
反応物4-MethylmorpholineHCID 7972—
反応物Phenyl ChlorodithioformateHCID 592675—
反応物N1-[2-(4-cyanophenoxy)-1-methylethyl]-L-valinamideHCID 22866848—
溶媒DichloromethaneHCID 6344—
生成物N1-[2-(4-cyanophenoxy)-1-methylethyl]-N2-phenoxycarbonyl-L-valinamideHCID 5371342066%

反応手順

0.5 g of N-methylmorpholine was added to a suspension containing 1.4 g of N1 -[2-(4-cyanophenoxy)-1-methylethyl]-L-valinamide suspended in 40 ml of methylene chloride, at -15° C. After 0.9 g of phenyl chlorodithioformate was added to the mixture at -15° C., the reaction mixture was allowed to sit and warm naturally to room temperature while being stirred, and subsequently the whole mixture was stirred for 15 hours at room temperature. Water was subsequently added to the reaction mixture. After the methylene chloride layer was washed with water, the organic layer was dried over anhydrous magnesium sulfate and the methylene chloride was removed under reduced pressure. The residue was purified by column chromatography on silica gel, thus yielding 1.4 g of the desired product in the form of a yellow glutinous substance (yield: 66%).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05811424
出典データセットuspto-grants-1998_09
ORD IDord-b83c5895d90b4eeeb48f095caf1ac85b
出典メモuspto-grants-1998_09