HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 848731Generated: October 26, 2026
3-Aminobenzamide → 3-[[2-[2-(3,4-Dimethoxyphenyl)ethylamino]-2-oxoethyl]amino]benzamide
https://huagongshe.com/reaction/848731
Participants
| Role | Name | HCID | Charge |
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| Reactant | 3-Aminobenzamide | HCID 1645 | — |
| Reactant | Sodium Iodide | HCID 5238 | — |
| Reactant | Calcium Carbonate | HCID 10112 | — |
| Reactant | 2-Chloro-N-(2-(3,4-dimethoxy-phenyl)-ethyl)-acetamide | HCID 26622 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 3-[[2-[2-(3,4-Dimethoxyphenyl)ethylamino]-2-oxoethyl]amino]benzamide | HCID 156651 | — |
Reaction Steps
100 ml of dimethylformamide was added to a mixture of 25.8 g of 2-chloro-N-(3,4-dimetoxyphenethyl)acetamide, 13.6 g of m-aminobenzamide, 15.0 g of sodium iodide and 20.0 g of calcium carbonate, and the mixture was stirred at 60° C. for 4 hours. The same procedure as described in Example 1 was followed to obtain 2-(3-carbamoylphenylamino)-N-(3,4-dimethoxyphenethyl)acetamide. The product was converted to the corresponding hydrochloride salt as described in Example 5. The salt was recrystallized from a mixture of methanol and diethyl ether to obtain 21.7 g of 2-(3-carbamoylphenylamino)-N-(3,4-dimethoxyphenethyl)acetamide hydrochloride having a melting point of 142°-155° C. (dec.).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04297357 |
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| Source dataset | uspto-grants-1981_10 |
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| ORD ID | ord-d127022fb13e40e8b21bad5422700896 |
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| Source note | uspto-grants-1981_10 |
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