HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 393181Generated: October 31, 2026
Potassium Carbonate → HCID 69929639, compound
https://huagongshe.com/reaction/393181
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | Pyrrolidine | HCID 31268 | — |
| Reactant | Dimethylformamide dimethyl acetal | HCID 78373 | — |
| Reactant | HCID 22649335 | HCID 22649335 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 69929639 | HCID 69929639 | — |
Reaction Steps
A mixture of 0.15 g of 6-fluoro-3-[1-[4-(4-fluorophenyl)-4-oxobutyl]piperidin-4-yl]benzo[b]thiophene hydrochloride, 0.05 g of anhydrous potassium carbonate, 0.36 ml of N,N-dimethylformamide dimethyl acetal, 0.25 ml of pyrrolidine and 0.5 ml of N,N-dimethylformamide was srirred on an oil bath at 120° C. for 3.5 hours. The reaction mixture was cooled to room temperature and then separated with ethyl acetate and water, and the aqueous layer was extracted with ethyl acetate. The combined organic layer was washed three times with a saturated aqueous sodium chloride solution. After drying over magnesium sulfate, the solvent was distilled off under reduced pressure to obtain crude 6-fluoro-3-[1-[3-(1-pyrrolidinomethylene)-4-(4-fluorophenyl)-4-oxobutyl]piperidin-4-yl]benzo[b]thiophene.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06806275B2 |
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| Source dataset | uspto-grants-2004_10 |
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| ORD ID | ord-25615e96d84f41bd8f19f0466b37adac |
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| Source note | uspto-grants-2004_10 |
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