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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1386256Generated: October 31, 2026

Hydrochloric Acid → 2-Amino-5-methoxy-4-(3-morpholinopropoxy)benzamide

https://huagongshe.com/reaction/1386256

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
Reactant5-Methoxy-4-(3-morpholinopropoxy)-2-nitrobenzamideHCID 21699285—
CatalystIronHCID 23925—
SolventMethanolHCID 887—
Product2-Amino-5-methoxy-4-(3-morpholinopropoxy)benzamideHCID 21699271—

Reaction Conditions

Temperature60 °C

Reaction Steps

Concentrated hydrochloric acid (30 ml) was added to a suspension of 5-methoxy-4-(3-morpholinopropoxy)-2-nitrobenzamide (5.67 g) in methanol (150 ml) and the mixture was heated to 60° C. When the 5-methoxy-4-(3-morpholinopropoxy)-2-nitrobenzamide had dissolved, iron powder (5.6 g, 100 mmol) was added in portions to the reaction mixture which was then heated for 90 minutes. After cooling, the insolubles were removed by filtration through diatomaceous earth, the volatiles were removed from the filtrate by evaporation and the residue was purified on a Diaion (trade mark of Mitsubishi) HP20SS resin column, eluting with water and then with hydrochloric acid pH2). Concentration of the fractions by evaporation gave a precipitate which was collected by filtration and dried under vacuum over phosphorus pentoxide to give 2-amino-5-methoxy-4-(3-morpholinopropoxy)benzamide as a hydrochloride salt (4.67 g, 75%) as beige crystals.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06265411B1
Source datasetuspto-grants-2001_07
ORD IDord-af96395ac1344e1db0d670dd10690698
Source noteuspto-grants-2001_07