HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1911369Generated: October 25, 2026
Cesium carbonate → Ethyl 5-(3,4-dimethylpiperazin-1-yl)thiophene-2-carboxylate
https://huagongshe.com/reaction/1911369
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Cesium carbonate | HCID 10796 | — |
| Reactant | Dimethylpiperazine | HCID 198037 | — |
| Reactant | Ethyl 5-bromothiophene-2-carboxylate | HCID 605723 | — |
| Reactant | Binap, (A+-)- | HCID 634876 | — |
| Catalyst | palladium(II) acetate | HCID 167845 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | Ethyl 5-(3,4-dimethylpiperazin-1-yl)thiophene-2-carboxylate | HCID 57440412 | 47.7% |
Reaction Steps
Palladium(II) acetate (0.112 g, 0.50 mmol) was added to a mixture of ethyl 5-bromothiophene-2-carboxylate (0.571 g, 5 mmol), 1,2-dimethyl-piperazine (1.175 g, 5 mmol), rac-2,2′-bis(diphenylphosphino)-1,1′-binaphthyl (0.311 g, 0.50 mmol) and cesium carbonate (2.281 g, 7.00 mmol) in toluene (50.0 ml) at 20° C. under nitrogen. The resulting suspension was stirred at 110° C. for 23 h. The crude product was purified by ion exchange chromatography, using a SCX2 column. The crude material was dissolved in methanol and then applied to the column. The desired product was eluted from the column using 2M NH3 in methanol and pure fractions were evaporated to dryness to afford the crude product as a brown oil. This material was further purified by silica column chromatography, eluting with a gradient of to 5% MeOH in DCM. Pure fractions were evaporated to dryness to afford ethyl 5-(3,4-dimethylpiperazin-1-yl)thiophene-2-carboxylate (0.640 g, 47.7%) as a light brown solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08604022B2 |
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| Source dataset | uspto-grants-2013_12 |
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| ORD ID | ord-56d8c49fe9424b1e8a1e6086bb477abf |
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| Source note | uspto-grants-2013_12 |
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