HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1420164Generated: October 25, 2026
Potassium Carbonate → Desfluoro Iloperidone (Impurity)
https://huagongshe.com/reaction/1420164
Participants
| Role | Name | HCID | Charge |
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| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 4-(3-Chloropropoxy)-3-methoxyacetophenone | HCID 7314264 | — |
| Reactant | 4-(3-Benzisothiazolyl) piperidine | HCID 13324093 | — |
| Catalyst | Potassium Iodide | HCID 4875 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | Desfluoro Iloperidone (Impurity) | HCID 10024423 | 109% |
Reaction Steps
A mixture of 3-(4-piperidinyl)-1,2-benzisothiazole (3.0 g, 13.7 mmol), potassium carbonate (2.3 g, 16.5 mmol), 1-[4-(3-chloropropoxy)-3-methoxyphenyl]ethanone (4.0 g, 16.5 mmol), potassium iodide (200 mg) and acetonitrile (100 ml) was stirred at reflux under N2 for 24 hours. The cooled reaction was filtered and the cake was washed well with acetonitrile. The filtrate was concentrated to an oily residue, which was partitioned between water and ethyl acetate. The ethyl acetate extract was washed well with water, dried with MgSO4 and concentrated to yield 6.1 g of a beige oil which solidified upon standing. The product was triturated with diethyl ether and filtered to give 4.2 g of a beige solid. The compound was recrystallized from ethyl alcohol to afford 3.5 g, and another recrystallization from ethyl alcohol (utilizing decolonizing carbon) provided 2.4 g (41%) of 1-[4-[3-[4-(1,2-benzisothiazol-3-yl)-1-piperidinyl]propoxy]-3-methoxyphenyl]ethanone, m.p. 93°-95° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05889004 |
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| Source dataset | uspto-grants-1999_03 |
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| ORD ID | ord-56dfc77dc39741189dbef56891ef9591 |
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| Source note | uspto-grants-1999_03 |
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