HuagongsheHuagongshe Chemistry Print Report · For research reference only
Hydrazine → 3,4-Dimethoxybenzamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Hydrazine | HCID 9321 | — |
| Reactant | HCID 24301347 | HCID 24301347 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | 3,4-Dimethoxybenzamide | HCID 73705 | 92.5% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08134015B2 |
| Source dataset | uspto-grants-2012_03 |
| ORD ID | ord-8c16232742404d8fb8eda07bb18da0aa |
| Source note | uspto-grants-2012_03 |