HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 915939Generated: October 29, 2026
1-Methylpiperazine → HCID 136005862, compound
https://huagongshe.com/reaction/915939
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 1-Methylpiperazine | HCID 53167 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | 1,3-Propanediamine, N'-(ethylcarbonimidoyl)-N,N-dimethyl-, monohydrochloride | HCID 2723939 | — |
| Reactant | HCID 136005769 | HCID 136005769 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 136005862 | HCID 136005862 | 75% |
Reaction Steps
To a 2 ml dichloromethane suspension of 86 mg (0.23 mmol) of the compound obtained in Example 65, 31 μl (0.28 mmol) of N-methylpiperazine and 53 mg (0.28 mmol) of 1-ethyl-3-(3-dimethylaminopropyl)carbodiimide hydrochloride were added, and the mixture was stirred at room temperature for 18 hours. Then, an aqueous solution of sodium hydrogen carbonate was added to the reaction mixture, and the mixture was extracted with dichloromethane. The organic layer was washed with water and a saturated aqueous solution of sodium chloride. After the washed layer was dried over anhydrous sodium sulfate, the solvent was distilled off under reduced pressure. The residue was purified by silica gel column chromatography (chloroform/methanol=20/1˜10/1) to obtain 80 mg (75%) of the captioned compound.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07268128B2 |
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| Source dataset | uspto-grants-2007_09 |
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| ORD ID | ord-b4fa832a764b46cf9985554ed7bb3e3e |
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| Source note | uspto-grants-2007_09 |
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