HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1172228Generated: October 27, 2026
N-(4-(2,2-Dicyanoethenyl)phenyl)acetamide → N-[4-(6-amino-5-cyano-2-mercapto-2,3-dihydropyrimidin-4-yl)phenyl]acetamide
https://huagongshe.com/reaction/1172228
Participants
| Role | Name | HCID | Charge |
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| Reactant | N-(4-(2,2-Dicyanoethenyl)phenyl)acetamide | HCID 33296 | — |
| Reactant | Thiourea | HCID 2723790 | — |
| Reactant | Sodium | HCID 5360545 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | N-[4-(6-amino-5-cyano-2-mercapto-2,3-dihydropyrimidin-4-yl)phenyl]acetamide | HCID 86621820 | 41.8% |
Reaction Steps
To 20 mL of absolute ethanol, 250 mg of metallic sodium was added in small portions. After dissolved completely, 760 mg of thiourea was added to the above solution, and the mixture was stirred at room temperature for 1 hour. To the reaction, 2.11 g of N-[4-(2,2-dicyanovinyl)phenyl]acetamide was added, and the mixture was heated to reflux for 3 hours. Then, the solvent was removed under reduced pressure from the reaction mixture, the residue was dissolved in 30 mL of water. In addition, the mixture was acidified by adding acetic acid in small portions, thereto 30 mL of ethyl acetate was added and then the solution was stirred overnight. Filtration of the precipitated material gave 1.2 g of N-[4-(6-amino-5-cyano-2-mercapto-2,3-dihydropyrimidin-4-yl)phenyl]acetamide as a white powder.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07834002B2 |
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| Source dataset | uspto-grants-2010_11 |
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| ORD ID | ord-0d7f92e212674c2f9cf27192a2404cf8 |
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| Source note | uspto-grants-2010_11 |
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