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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 359726생성일: 2026년 10월 24일

Hydrochloric Acid → N,N-dimethyl 3-indolepyruvamide

https://huagongshe.com/ko/reaction/359726

반응식

참여 물질

역할이름HCID투입량
반응물Hydrochloric AcidHCID 313—
반응물DimethylamineHCID 674—
반응물Indole-3-pyruvic acidHCID 803—
반응물HCID 178418300HCID 178418300—
촉매GoldHCID 23985—
용매DichloromethaneHCID 6344—
용매4-MethylmorpholineHCID 7972—
용매TetrahydrofuranHCID 8028—
생성물N,N-dimethyl 3-indolepyruvamideHCID 53877758—

반응 단계

A solution of 500 mg 3-indolepyruvic acid in 25 ml anhydrous tetrahydrofuran on an ice-salt bath, under argon atmosphere and under stirring was additioned in swift succession with: 400 mg hydroxybenzotriazole (HOBt) and 570 mg 1-(3-dimethylaminopropyl)-3-ethylcarbimdie.HCl (EDC.HCl). After dissolving and still maintaining the ice-salt bath, 240 mg dimethylamine.HCl were added dissolved in 10 ml anhydrous tetrahydrofuran and 325 microliters 4-methylmorpholine (NMM). The yellowish gold solution was maintained under stirring for one night, leaving the bath temperature to rise up to room temperature. The volume was then tripled adding CH2Cl2 and the organic solution was washed in sequence with 5% NaHCO3 (10×25 ml), saturated NaCl solution (3×25 ml), 5% KHSO4 (10×25 ml) and saturated NaCl solution up to neutrality. After standing for one night on anhydrous Na2SO4, this was filtered off, the mixture was purified by flash chromatography (silica gel, eluent CH2Cl2 25/n-propanol 1,5).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05002963
출처 데이터셋uspto-grants-1991_03
ORD IDord-0086fdaf794944df91060ca4940e1dca
출처 메모uspto-grants-1991_03