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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 580131Generated: October 27, 2026

Dimethylformamide → 1,3-Propanediamine, N,N-diethyl-N'-(1H-indazol-3-yi)-

https://huagongshe.com/reaction/580131

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethylformamideHCID 6228—
ReactantPotassium CarbonateHCID 11430—
Reactant1H-indazol-3-amineHCID 13399—
Reactant(3-Bromopropyl)diethylamine hydrobromideHCID 12639158—
SolventWaterHCID 962—
SolventChloroformHCID 6212—
Product1,3-Propanediamine, N,N-diethyl-N'-(1H-indazol-3-yi)-HCID 306804352%

Reaction Conditions

Temperature80 °C

Reaction Steps

To 80 ml of anhydrous N,N-dimethylformamide were added 4 g of 3-aminoindazole as prepared in accordance with the method described in C. E. Kwartler et al., J. Am. Chem. Soc., 65, 1804 (1943), 8.3 g of 3-bromopropyldiethylamine hydrobromide and 8.3 g of anhydrous potassium carbonate. The mixture was stirred for 24 hours at 80° C. and condensed under reduced pressure. To the condensed residue were added 100 ml of chloroform and 50 ml of water. The chloroform layer was dried over anhydrous sodium sulfate, and chloroform was removed under reduced pressure. The residue thus obtained was subjected to an alumina-column chromatography(alumina: 200 g) using chloroform as the developing solvent to give 3.85 g of 3-(3-diethylaminopropylamino)indazole having the following analytical values in a yield of 52%.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04751302
Source datasetuspto-grants-1988_06
ORD IDord-83b33f51523541bf852c87362a033069
Source noteuspto-grants-1988_06