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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 67405생성일: 2026년 10월 24일

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

https://huagongshe.com/ko/reaction/67405

반응식

참여 물질

역할이름HCID투입량
반응물Hydrochloric AcidHCID 313—
반응물GlycineHCID 750—
반응물Sodium ChlorideHCID 5234—
반응물Isatoic AnhydrideHCID 8359—
반응물Sodium HydroxideHCID 14798—
반응물2,4-DimethoxybenzaldehydeHCID 69175—
반응물(2,4-Dimethoxy-benzylamino)-acetic acidHCID 11042399—
촉매PalladiumHCID 23938—
용매Dimethyl SulfoxideHCID 679—
용매MethanolHCID 887—
용매WaterHCID 962—
생성물(2,4-Dimethoxy-benzylamino)-acetic acidHCID 11042399—
생성물3,4-dihydro-4-(2,4-dimethoxybenzyl)-2H-1,4-benzodiazepine-2,5(1H)-dioneHCID 21764314—

반응 단계

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.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04346032
출처 데이터셋uspto-grants-1982_08
ORD IDord-39334f19e71744d793e29b729d245f50
출처 메모uspto-grants-1982_08