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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 359726Generated: October 27, 2026

Hydrochloric Acid → N,N-dimethyl 3-indolepyruvamide

https://huagongshe.com/reaction/359726

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantDimethylamineHCID 674—
ReactantIndole-3-pyruvic acidHCID 803—
ReactantHCID 178418300HCID 178418300—
CatalystGoldHCID 23985—
SolventDichloromethaneHCID 6344—
Solvent4-MethylmorpholineHCID 7972—
SolventTetrahydrofuranHCID 8028—
ProductN,N-dimethyl 3-indolepyruvamideHCID 53877758—

Reaction Steps

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).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05002963
Source datasetuspto-grants-1991_03
ORD IDord-0086fdaf794944df91060ca4940e1dca
Source noteuspto-grants-1991_03