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HRID 67405作成日:2026年10月25日

Hydrochloric Acid → (2,4-Dimethoxy-benzylamino)-acetic acid

https://huagongshe.com/reaction/67405

反応式

関与物質

役割名称HCID仕込み量
反応物Hydrochloric AcidHCID 313—
反応物GlycineHCID 750—
反応物Sodium ChlorideHCID 5234—
反応物Isatoic AnhydrideHCID 8359—
反応物Sodium HydroxideHCID 14798—
反応物2,4-DimethoxybenzaldehydeHCID 69175—
反応物(2,4-Dimethoxy-benzylamino)-acetic acidHCID 11042399—
触媒PalladiumHCID 23938—
溶媒Dimethyl SulfoxideHCID 679—
溶媒MethanolHCID 887—
溶媒WaterHCID 962—
生成物(2,4-Dimethoxy-benzylamino)-acetic acidHCID 11042399—
生成物3,4-dihydro-4-(2,4-dimethoxybenzyl)-2H-1,4-benzodiazepine-2,5(1H)-dioneHCID 21764314—

反応手順

N-(2,4-dimethoxybenzyl)glycine is prepared by the reaction of glycine with 2,4-dimethoxybenzaldehyde in the presence of sodium hydroxide, reduction with palladium-on-carbon in methanol and subsequent neutralisation with 2 N hydrochloric acid. The aqueous solution obtained is concentrated. 41.9 g of this mixture of N-(2,4-dimethoxybenzyl)-glycine and sodium chloride are stirred at 110° C. for 1.5 hours in 300 ml of dimethyl sulphoxide with 23.18 g (142 mmol) of isatoic acid anhydride. The mixture is poured into ca 2 liters of water and stirred for 0.5 hour. The separated crystals are filtered off under suction, washed with water and dried. After recrystallisation from ethyl acetate, there is obtained 3,4-dihydro-4-(2,4-dimethoxybenzyl)-2H-1,4-benzodiazepine-2,5(1H)-dione of melting point 151°-152.5° C.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US04346032
出典データセットuspto-grants-1982_08
ORD IDord-39334f19e71744d793e29b729d245f50
出典メモuspto-grants-1982_08