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HRID 2288362作成日:2026年10月27日

4-Methylamino-3-chloracetamidobenzoic acid-n-(n-propyl)-n-(2-ethoxycarbonylethyl)amide → 2-Chloromethyl-1-methylbenzimidazol-5-yl-carboxylic acid-n-(n-propyl)-n-(2-ethoxycarbonylethyl)amide

https://huagongshe.com/reaction/2288362

反応式

関与物質

役割名称HCID仕込み量
反応物4-Methylamino-3-chloracetamidobenzoic acid-n-(n-propyl)-n-(2-ethoxycarbonylethyl)amideHCID 18412409—
溶媒Acetic AcidHCID 176—
生成物2-Chloromethyl-1-methylbenzimidazol-5-yl-carboxylic acid-n-(n-propyl)-n-(2-ethoxycarbonylethyl)amideHCID 18412376—

反応手順

1.6 g (4.3 mMol) of 4-methylamino-3-chloracetamido-benzoic acid-N-(n-propyl)-N-(2-ethoxycarbonylethyl)-amide were heated to 100° C. in 25 ml of acetic acid for 30 minutes. Then the solvent was distilled off, the crude product was taken up in 40 ml methylene chloride/ethanol (9:1) and washed with 20 ml saturated sodium hydrogen carbonate solution. The organic phase was dried with sodium sulphate and evaporated down. Yield: 1.5 g (100% of theory) of brown oil, Rf value: 0.63 (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-d2ac45776610487695402fea17528042
出典メモuspto-grants-2000_07