HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 420568Generated: October 30, 2026
Dimethylformamide → [4-(5-Bromothiazole-2-yl)-2,6-dimethyl piperazine-1-yl]acetic acid methyl ester
https://huagongshe.com/reaction/420568
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Dimethylformamide | HCID 6228 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | Methyl bromoacetate | HCID 60984 | — |
| Reactant | 1-(5-Bromothiazole-2-yl)-3,5-dimethyl piperazine | HCID 66657911 | — |
| Solvent | Water | HCID 962 | — |
| Product | [4-(5-Bromothiazole-2-yl)-2,6-dimethyl piperazine-1-yl]acetic acid methyl ester | HCID 66657554 | 74% |
Reaction Steps
A mixture of 1-(5-bromothiazole-2-yl)-3,5-dimethyl piperazine (21.5 g), bromo acetic acid methyl ester (8.8 mL), potassium carbonate (12.9 g) and dimethylformamide (150 mL) was stirred at 60° C. for 2.5 hours. To the reaction solution was added water and extracted with ethyl acetate. The organic layer was washed with water and brine, and dried over magnesium sulphate. The solvent was evaporated under reduced pressure. The residue was purified by column chromatograph on silica gel to give the title compound (20.1 g). Yield: 74%.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08097610B2 |
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| Source dataset | uspto-grants-2012_01 |
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| ORD ID | ord-4b0c471c13cf41f4a78151cb8d894c33 |
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| Source note | uspto-grants-2012_01 |
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