Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | 1H-Pyrrolo(2,3-b)pyridine | HCID 9222 | — |
| Reactant | Cesium carbonate | HCID 10796 | — |
| Reactant | 1-BENZYL-3-CHLORO-PIPERIDINE | HCID 12275351 | — |
| Solvent | Dimethyl Sulfoxide | HCID 679 | — |
| Product | HCID 22065940 | HCID 22065940 | 60% |
Reaction Steps
A mixture of 1-benzyl-3-chloropiperidine (3.83 g, 18.3 mmol), 1H-pyrrolo[2,3-b]pyridine (4.4 g, 36.5 mmol) and cesium carbonate (17.8 g, 54.8 mmol) in DMSO is stirred at 80° C. under a nitrogen atmosphere for 24 h. The reaction is monitored by thin layer chromatography. Two additional amounts of 1-benzyl-3-chloro-piperidine (3.83 g and 1.91 g) are added at 12 h intervals. After 48 h, the mixture is cooled, treated with water and extracted with ethyl acetate. The extracts are combined, washed sequentially with water and brine and concentrated in vacuo. The resultant residue is purified by flash chromatography (4-5% methanol in CH2Cl2 as eluent) to afford the title compound as an oil, 6.5 g (60% yield), identified by HNMR and mass spectral analyses.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07411064B2 |
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| Source dataset | uspto-grants-2008_08 |
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| ORD ID | ord-c2198fb8a230472692186f1eab7525f9 |
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| Source note | uspto-grants-2008_08 |
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