HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 417976Generated: October 31, 2026
Diisopropylethylamine → HCID 42635797, compound
https://huagongshe.com/reaction/417976
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | HCID 20099350 | HCID 20099350 | — |
| Reactant | 2-(4-Methylpiperazin-1-yl)ethyl 4-nitrophenyl carbonate | HCID 57445007 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 42635797 | HCID 42635797 | 69.4% |
Reaction Steps
2-(4-Methylpiperazin-1-yl)ethyl 4-nitrophenyl carbonate (Intermediate 4; 2.56 g, 8.28 mmol) was dissolved in DMF (20 mL). DIPEA (1.40 mL, 8.45 mmol) and 2-Methyl-4-(3-methylphenyl)piperazine (1.50 g, 7.87 mmol) were added and the reaction mixture was stirred at room temperature for 24 hours, and the reaction mixture was then concentrated in vacuo. The resulting residue was dissolved in EtOAc (200 mL) and washed with 1 M aq Na2CO3 solution (6×100 mL), dried (MgSO4) and concentrated in vacuo. The residue was purified by reverse phase chromatography (gradient eluting with MeOH in water, with 1% formic acid in each solvent, 0-30%). The resulting residue was dissolved in DCM (50 mL) and stirred with solid K2CO3 for 20 minutes, filtered and concentrated in vacuo, give 2-(4-methylpiperazin-1-yl)ethyl 3-methyl-4-(3-methylphenyl)piperazine-1-carboxylate (1.97 g, 69%) as a pale yellow oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08093248B2 |
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| Source dataset | uspto-grants-2012_01 |
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| ORD ID | ord-f81de825ccf344969ed1818d3fef463c |
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| Source note | uspto-grants-2012_01 |
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