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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1094996Generated: November 3, 2026

Hydrazine → 3,4-Dimethoxybenzamide

https://huagongshe.com/reaction/1094996

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrazineHCID 9321—
ReactantHCID 24301347HCID 24301347—
SolventEthanolHCID 702—
Product3,4-DimethoxybenzamideHCID 7370592.5%

Reaction Steps

Subsequently, 2-(3,4-dimethoxy-benzoylamino)-5-methyl-thiophene-3-carboxylic acid methyl ester (16 mg) synthesized by the above process was dissolved in ethanol (5 ml). Hydrazine (1 ml) was then added to the solution at room temperature, and the mixture was stirred at that temperature for 12 hr. After the completion of the reaction, the reaction system was concentrated under the reduced pressure, and the residue was purified by column chromatography eluted with a chloroform-methanol system to give N-(3-hydrazinocarbonyl)-5-methylthiophen-2-yl)-3,4-dimethoxy-benzamide (8.0 mg, yield 50%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08134015B2
Source datasetuspto-grants-2012_03
ORD IDord-8c16232742404d8fb8eda07bb18da0aa
Source noteuspto-grants-2012_03