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HRID 2288361作成日:2026年10月25日

Chloroacetic Acid → 4-Methylamino-3-chloracetamidobenzoic acid-n-(n-propyl)-n-(2-ethoxycarbonylethyl)amide

https://huagongshe.com/reaction/2288361

反応式

関与物質

役割名称HCID仕込み量
反応物Chloroacetic AcidHCID 300—
反応物3-amino-4-ethylaminobenzoic acid-N-phenyl-N-(2-ethoxycarbonylethyl)amideHCID 18412523—
反応物3-Amino-4-methylaminobenzoic acid-n-(n-propyl)-n-(2-ethoxycarbonylethyl)amideHCID 18412526—
溶媒TetrahydrofuranHCID 8028—
生成物4-Methylamino-3-chloracetamidobenzoic acid-n-(n-propyl)-n-(2-ethoxycarbonylethyl)amideHCID 18412409—

反応手順

A solution of 1.8 g (5.9 mMol) of 3-amino-4-methylamino-benzoic acid-N-(n-propyl)-N-(2-ethoxycarbonylethyl)-amide [prepared analogously to 3-amino-4-ethylamino-benzoic acid-N-phenyl-N-(2-ethoxycarbonylethyl)-amide], 1.1 g (6.8 mMol) of N,N'-carbonyldiimidazole and 0.65 g (6.9 mMol) of chloroacetic acid in 75 ml tetrahydrofuran was stirred for 1 hour at room temperature. Then the solvent was distilled off in vacuo, and the crude product was purified by flash chromatography (silica gel; methylene chloride/ethanol=49:1). Yield: 1.7 g (77% of theory) yellow oil, Rf value: 0.58 (silica gel; ethyl acetate/ethanol/ammonia=90:10:1)

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06087380
出典データセットuspto-grants-2000_07
ORD IDord-1b6612ff2aff4cfdb2cef3e2ddab8afd
出典メモuspto-grants-2000_07