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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 60160Generated: October 25, 2026

1-Ethyl-3-(3'-dimethylaminopropyl)carbodiimide → 5-amino-N-(3-(tert-butyldimethylsilyloxy)propyl)-2-chloroisonicotinamide

https://huagongshe.com/reaction/60160

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-Ethyl-3-(3'-dimethylaminopropyl)carbodiimideHCID 15908—
Reactant1-HydroxybenzotriazoleHCID 75771—
Reactant(3-Aminopropoxy)(tert-butyl)dimethylsilaneHCID 11074190—
Reactant5-Amino-2-chloro-isonicotinic acidHCID 22736791—
SolventWaterHCID 962—
SolventDimethylformamideHCID 6228—
SolventEthyl AcetateHCID 8857—
Product5-amino-N-(3-(tert-butyldimethylsilyloxy)propyl)-2-chloroisonicotinamideHCID 13173707943.1%

Reaction Steps

To a solution of 5-amino-2-chloroisonicotinic acid (5 g, 0.029 mol) in DMF (40 mL) was added EDCI (8.34 g, 0.0435 mol) and HOBT (5.87 g, 0.0435 mol). The reaction was stirred at RT for 30 min then 3-(tert-butyldimethylsilyloxy)propan-1-amine (5.5 g, 0.029 mol) was added. The reaction was stirred at RT for 5 h then poured in EA (50 mL) and water (20 mL). The organic layer was washed with brine (50 mL), dried over Na2SO4 and concentrated to a residue which was purified by chromatography eluted with PE/EA (2:1) to give 5-amino-N-(3-(tert-butyldimethylsilyloxy)propyl)-2-chloroisonicotinamide (4.3 g, 43% yield) as a white solid. LCMS: MH+ 344 and TR=1.877 min.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09440973B2
Source datasetuspto-grants-2016_09
ORD IDord-794b798882284710a7860b0bd603612c
Source noteuspto-grants-2016_09