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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 20991Generated: October 26, 2026

Water → 1-(Tert-butoxycarbonyl)-5-(3-dimethylamino-2-propyn-1-yl)indole

https://huagongshe.com/reaction/20991

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantN,N-DimethylpropargylamineHCID 81643—
Reactant5-Iodo-1H-indole, N-BOC protectedHCID 16125958—
CatalystHCID 178418476HCID 178418476—
SolventDiethylamineHCID 8021—
Product1-(Tert-butoxycarbonyl)-5-(3-dimethylamino-2-propyn-1-yl)indoleHCID 6849342990%

Reaction Conditions

Temperature80 °C

Reaction Steps

1-(tert-Butoxycarbonyl)-5-iodoindole (1.00 g, 2.91 mmol) was dissolved in diethylamine (20 mL), and the solution was added with bis(triphenylphosphine)dichloropalladium (163 mg, 0.233 mmol), cuprous iodide (44.4 mg, 0.233 mmol) and 1-dimethylamino-2-propyne (0.628 mL, 5.82 mmol), followed by stirring at 80° C. for 7.0 hours. The reaction mixture was added with water and extracted with ethyl acetate. The organic layer was washed with saturated brine and dried over anhydrous sodium sulfate. The solvent was evaporated under reduced pressure. The residue was purified by preparative thin-layer chromatography (chloroform/methanol=19/1) to obtain 1-(tert-butoxycarbonyl)-5-(3-dimethylamino-2-propyn-1-yl)indole (0.78 g, yield 90%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07745641B2
Source datasetuspto-grants-2010_06
ORD IDord-a8a7964606714175a8ec31928416e35e
Source noteuspto-grants-2010_06