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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 464820Generated: October 25, 2026

Dimethylformamide → 1-(3-Diethylaminopropyl)-3-(3-diethylaminopropylamino)indazole

https://huagongshe.com/reaction/464820

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethylformamideHCID 6228—
ReactantPotassium CarbonateHCID 11430—
Reactant1H-Indazole-1-propanamine, 3-amino-N,N-diethyl-HCID 3028893—
Reactant(3-Bromopropyl)diethylamine hydrobromideHCID 12639158—
SolventWaterHCID 962—
SolventChloroformHCID 6212—
Product1-(3-Diethylaminopropyl)-3-(3-diethylaminopropylamino)indazoleHCID 303083752.2%

Reaction Conditions

Temperature80 °C

Reaction Steps

To 60 ml of anhydrous N,N-dimethylformamide were added 4.00 g of 1-(3-diethylaminopropyl)-3-aminoindazole prepared by the same method as Example 26, 8.98 g of 3-bromopropyldiethylamine hydrobromide and 7.89 g of anhydrous potassium carbonate, and the mixture was stirred for 12 hours at 80° C. After cooling the reaction mixture, the mixture was added with 80 ml of water and extracted with diethyl ether. Then the ether layer was extracted three times with 2N-hydrochloric acid. The hydrochloric acid layer was washed with diethyl ether and the pH of the layer was adjusted to 14 with potassium carbonate. The layer was extracted three times with chloroform. The chloroform layer was dried with 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 solvent to give 3.05 g of 1-(3-diethylaminopropyl)-3-(3-diethylaminopropylamino)indazole in a yield of 52%.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04549023
Source datasetuspto-grants-1985_10
ORD IDord-62b0ae6c60cd4d9db919324b236cf652
Source noteuspto-grants-1985_10