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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 580152Generated: October 25, 2026

Ammonia → 1-(3-Diethylaminopropyl)-3-(3-diethylaminopropylamino)-5-aminoindazole

https://huagongshe.com/reaction/580152

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAmmoniaHCID 222—
ReactantHydrochloric AcidHCID 313—
ReactantNitric AcidHCID 944—
Reactant1-(3-Diethylaminopropyl)-3-(3-diethylaminopropylamino)indazoleHCID 3030837—
CatalystIronHCID 23925—
SolventBenzeneHCID 241—
SolventWaterHCID 962—
SolventSulfuric AcidHCID 1118—
SolventChloroformHCID 6212—
Product1-(3-Diethylaminopropyl)-3-(3-diethylaminopropylamino)-5-aminoindazoleHCID 2013583749%

Reaction Steps

In 2.58 ml of sulfuric acid was dissolved 1.7 g of the 1-(3-diethylaminopropyl)-3-(3-diethylaminopropyl-amino)indazole. To the solution were added dropwise 0.41 ml of nitric acid(d =1.42) and 0.41 ml of sulfuric acid (specific gravity 1.84) under cooling with ice. The solution was stirred for 2 hours at 5°-10° C. and added to 12.1 ml of ice and water. The pH of the solution was adjusted to at least 11 with an aqueous ammonia solution, and the solution was extracted with chloroform. The chloroform layer was dried over anhydrous sodium sulfate and chloroform was removed under reduced pressure. The residue thus obtained was dissolved in 50 ml of dried benzene. To the solution were added 10 g of iron powder and 2 ml of hydrochloric acid, and the mixture was stirred for 30 minutes at 80° C. To the mixture was added 0.5 ml of water, and the mixture was stirred for 10 hours at 80° C. After cooling, the mixture was filtered, and the benzene layer was extracted three times with 20 ml of 1N hydrochloric acid. The pH of the hydrochloric acid layer was adjusted to at least 11 with potassium carbonate, and the alkali layer was extracted with chloroform. 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: 100 g) using chloroform as the developing solvent to give 0.87 g of 1-(3-diethylaminopropyl)-3-(3-diethylaminopropylamino)-5-aminoindazole having the following analytical values in a yield of 49%.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04751302
Source datasetuspto-grants-1988_06
ORD IDord-07229cf2c2d44040bcb4ac089b36ddd1
Source noteuspto-grants-1988_06