Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 5-Chloro-1,3-dihydro-1-(4-piperidinyl)-2H-benzimidazol-2-one | HCID 104607 | — |
| Reactant | HCID 13151500 | HCID 13151500 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 86739107 | HCID 86739107 | — |
Reaction Steps
A mixture of 5.2 g of trans-2-(4-fluorophenyl)-4-(iodomethyl)tetrahydrofuran, 4.3 g of 1-(4-piperidyl)-5-chloro-benzimidazolin-2-one and 2.3 g of potassium carbonate in 50 ml of dimethylformamide is heated with stirring at 70° C. for 24 hours. The reaction mixture is then poured into water and extracted with ethyl acetate. The extract is washed with water and dried over magnesium sulfate, and the solvent is distilled off under reduced pressure. The residue is dissolved in a small amount of chloroform, and a solution of 0.8 g of maleic acid in ethanol is added thereto. The crystals precipitated are collected by filtration and recrystallized from methanol to give 1-[1-(trans-2-(4-fluorophenyl)-tetrahydro-4-furylmethyl)-4-piperidyl]-5-chloro-benzimidazolin-2-one maleate, melting at 208.5°-209° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04414216 |
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| Source dataset | uspto-grants-1983_11 |
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| ORD ID | ord-8a86ef657d12404ca5e4f35fa4e3035b |
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| Source note | uspto-grants-1983_11 |
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