HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1890812Generated: November 1, 2026
Ethylene Glycol → tert-butyl 4-(1-methyl-1H-pyrazol-4-yl)-3-oxopiperazine-1-carboxylate
https://huagongshe.com/reaction/1890812
Participants
| Role | Name | HCID | Charge |
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| Reactant | Ethylene Glycol | HCID 174 | — |
| Reactant | Potassium Phosphate, Tribasic | HCID 62657 | — |
| Reactant | 1-Methyl-4-iodo-1H-pyrazole | HCID 2734773 | — |
| Reactant | Tert-butyl 3-oxopiperazine-1-carboxylate | HCID 3157178 | — |
| Catalyst | Copper iodide | HCID 83717 | — |
| Solvent | Isopropanol | HCID 3776 | — |
| Product | tert-butyl 4-(1-methyl-1H-pyrazol-4-yl)-3-oxopiperazine-1-carboxylate | HCID 67153719 | — |
Reaction Steps
tert-Butyl 3-oxopiperazine-1-carboxylate (0.164 g, 0.819 mmol) was suspended in isopropanol (3 mL) under an atmosphere of nitrogen and treated with 1-methyl-4-iodo-1H-pyrazole (0.204 g, 0.983 mmol, 1.20 equiv), ethylene glycol (0.051 g, 0.82 mmol, 1.0 equiv), copper iodide (0.031 g, 0.16 mmol, 0.20 equiv), and potassium phosphate (0.695 g, 3.28 mmol, 4.00 equiv), and placed into a preheated oil bath at 100° C. for 8 hours. The mixture was cooled to ambient temperature, concentrated in vacuo and the residue was dissolved in dichloromethane, washed with water, dried with sodium sulfate, filtered, and concentrated in vacuo. The residue was purified by silica gel chromatography (100:0 to 0:100 hexanes:ethyl acetate), providing the titled compound.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08507494B2 |
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| Source dataset | uspto-grants-2013_08 |
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| ORD ID | ord-fafb75c317704ee8b599046f05fc0984 |
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| Source note | uspto-grants-2013_08 |
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