HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 266063Generated: November 1, 2026
4-(4-Methoxyphenyl)-1-piperazinecarboximidamide → HCID 19032445, compound
https://huagongshe.com/reaction/266063
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 4-(4-Methoxyphenyl)-1-piperazinecarboximidamide | HCID 4741189 | — |
| Reactant | Sodium Methoxide | HCID 10942334 | — |
| Reactant | HCID 14786861 | HCID 14786861 | — |
| Solvent | Methanol | HCID 887 | — |
| Solvent | 1-Propanol | HCID 1031 | — |
| Product | HCID 19032445 | HCID 19032445 | 62.5% |
Reaction Steps
To a mixture of 20 g of 4-(4-methoxyphenyl)-1-piperazinecarboximidamide and 21 g of N-[3-(dimethylamino)methylene]amino]-2-propenylidene]-N-methylmethanaminium perchlorate in 200 ml of 1-propanol were added dropwise 70 ml of a solution of sodium methoxide in methanol (1M). After stirring for 2 hours there were added dropwise again 70 ml of a solution of sodium methoxide in methanol (1M). Then the mixture was stirred and refluxed for 2 hours. After cooling, the reaction mixture was evaporated and the residue was purified by column chromatography (eluent: CH2Cl2 /CH3OH 97:3). The eluent of the desired fraction was evaporated, yielding 15 g (62.5%) of N-[(dimethylamino)methylene]-2-[4-(4-methoxyphenyl)-1-piperazinyl]-5-pyrimidinamine (interm. 24);
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05650411 |
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| Source dataset | uspto-grants-1997_07 |
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| ORD ID | ord-4d52551ec1ff4d99afe9ddaf2fd11934 |
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| Source note | uspto-grants-1997_07 |
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