HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 633313Generated: October 29, 2026
Potassium Carbonate → HCID 58614845, compound
https://huagongshe.com/reaction/633313
Participants
| Role | Name | HCID | Charge |
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| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 1-Acetylpiperazine | HCID 83795 | — |
| Reactant | HCID 66877367 | HCID 66877367 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 58614845 | HCID 58614845 | 33.2% |
Reaction Steps
3-(2-Bromoethoxy)-N-(4-chloro-3-(pyridin-2-yl)phenyl)-4-(methylsulfonylmethyl)benzamide (50 mg, 0.095 mmol) was dissolved in DMF (1.0 ml) and treated with potassium carbonate (18 mg, 0.13 mmol) and 1-(piperazin-1-yl)ethanone (15 mg, 0.11 mmol) for 18 hours. The reaction was heated for 2.0 hours at 50° C., then additional potassium carbonate (18 mg, 0.13 mmol) and 1-(piperazin-1-yl)ethanone (15 mg, 0.11 mmol) was added. After 2 hours, the reaction was quenched in 5% NaOH and extracted with ethyl acetate twice. The ethyl acetate extracts were washed with water once, brine once, dried with MgSO4, and purified by reverse phase HPLC to yield 18 mg of 3-(2-(4-acetylpiperazin-1-yl)ethoxy)-N-(4-chloro-3-(pyridin-2-yl)phenyl)-4-(methylsulfonylmethyl)benzamide. MS (Q1) 543 (M)+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09321761B2 |
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| Source dataset | uspto-grants-2016_04 |
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| ORD ID | ord-5e77d3c2067f47c6bfa0040138277ed9 |
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| Source note | uspto-grants-2016_04 |
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