Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Potassium Iodide | HCID 4875 | — |
| Reactant | Acetonitrile | HCID 6342 | — |
| Reactant | Piperidin-3-ylmethanol | HCID 107308 | — |
| Reactant | 5-(3-Chloropropyl)-10,11-dihydro-5H-dibenz[b,f]azepine | HCID 286779 | — |
| Solvent | Water | HCID 962 | — |
| Product | HCID 22998314 | HCID 22998314 | 61% |
Reaction Steps
A mixture of 3-(hydroxymethyl)piperidine (1.01 g, 0.0088 mol), acetonitrile (9 ml), 5-(3-chloropropyl)-10,11-dihydro-5H-dibenzo[b,f]azepine (0.86 g, 0.003 mol, pre-pared similarly as described in example 1) and potassium iodide (0.56 g, 0.003 mol) was heated at reflux temperature for 18 h. Water (20 ml) was added, and the mixture was extracted with ethyl acetate (3×15 ml). The combined organic extracts were washed with brine (2×20 ml), dried (MgSO4) and concentrated in vacuo. The residue was redissolved in a mixture of water (20 ml) and concentrated hydrochloric acid (3 ml), and extracted with dichlorometyhane (3×10 ml). The combined organic extracts were washed with brine (20 ml), dried (MgSO4) and concentrated in vacuo. The residue was crystallised from a mixture of methanol (0.5 ml) and ethyl acetate (5 ml), affording 0.8 g (61%) of the title compound as needles.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06239148B1 |
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| Source dataset | uspto-grants-2001_05 |
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| ORD ID | ord-0b84ec0afb1340de81fb595cd908293e |
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| Source note | uspto-grants-2001_05 |
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