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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 580140Generated: October 27, 2026

Dimethylformamide → N~1~,N~1~-Diethyl-N~3~-(5-iodo-1H-indazol-3-yl)propane-1,3-diamine

https://huagongshe.com/reaction/580140

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethylformamideHCID 6228—
ReactantPotassium CarbonateHCID 11430—
Reactant(3-Bromopropyl)diethylamine hydrobromideHCID 12639158—
Reactant3-Amino-5-iodo-1H-indazoleHCID 20135868—
SolventWaterHCID 962—
SolventChloroformHCID 6212—
ProductN~1~,N~1~-Diethyl-N~3~-(5-iodo-1H-indazol-3-yl)propane-1,3-diamineHCID 2013584863.6%

Reaction Conditions

Temperature80 °C

Reaction Steps

To 80 ml of anhydrous N,N-dimethylformamide were added 9.7 g of 3-amino-5-iodoindazole as prepared in accordance with the method described in C. E. Kwartler et el., 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. The condensed residue was added with 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 7.15 g of 3-(3-diethylaminopropylamino)-5-iodoindazole having the following analytical values in a yield of 51%.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04751302
Source datasetuspto-grants-1988_06
ORD IDord-f1c3ede0cc2148358f4432bb8bf38e8c
Source noteuspto-grants-1988_06