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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1791541Generated: October 25, 2026

Hydrochloric Acid → 2-Amino-5-methoxy-4-(3-(pyrrolidin-1-yl)propoxy)benzamide hydrochloride

https://huagongshe.com/reaction/1791541

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
Reactant5-Methoxy-2-nitro-4-(3-(pyrrolidin-1-yl)propoxy)benzamideHCID 21874822—
CatalystIronHCID 23925—
SolventMethanolHCID 887—
Product2-Amino-5-methoxy-4-(3-(pyrrolidin-1-yl)propoxy)benzamide hydrochlorideHCID 2187482085%

Reaction Conditions

Temperature50 °C

Reaction Steps

Concentrated hydrochloric acid (5 ml) was added to a suspension of 5-methoxy-2-nitro-4-(3-(pyrrolidin-1-yl)propoxy)benzamide (1.5 g, 4.64 mmol) in methanol (20 ml) and the mixture was heated at 50° C. to give a solution. Iron powder (1.3 g, 23.2 mmol) was added in portions and the reaction mixture was then heated at reflux for 1 hour. The mixture was allowed to cool, the insolubles were removed by filtration through diatomaceous earth and the volatiles were removed from the filtrate by evaporation. The residue was purified on a Diaion (trade mark of Mitsubishi) HP20SS resin column, eluting with water and then with dilute hydrochloric acid (pH2). The fractions containing product were concentrated by evaporation and the resulting precipitate was collected by filtration and dried under vacuum over phosphorus pentoxide to give 2-amino-5-methoxy-4-(3-(pyrrolidin-1-yl)propoxy)benzamide hydrochloride (1.44 g, 85%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07074800B1
Source datasetuspto-grants-2006_07
ORD IDord-65c85e4819d640f5a613400a453478e4
Source noteuspto-grants-2006_07