Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Potassium Iodide | HCID 4875 | — |
| Reactant | 2-Fluoroethyl p-Toluenesulfonate | HCID 256019 | — |
| Reactant | HCID 10081651 | HCID 10081651 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 59526803 | HCID 59526803 | 50.2% |
Reaction Steps
Potassium iodide (0.71 g, 4.27 mmol) and 2-fluoroethyl 4-methylbenzenesulfonate (0.93 g, 4.27 mmol) (Kopka, et al., 2006) are added to a solution of (S)-1-((R)-1-benzylpyrrolidin-3-yl)ethanamine (0.83 g, 4.06 mmol) (Shroeder, et al., 1992) in DMF (10 mL). The reaction mixture is heated for 2 h at 100° C. and evaporated under reduced pressure. The residue is purified by column chromatography (chloroform-ethanol-triethylamine=30:1:1) to afford the desired product (0.51 g, 50%) as a brown oil. 1H NMR (CDCl3): δ 1.09 (d, J=6.3 Hz, 3H, methyl), 1.55 (m, 1H), 1.96 (m, 1H), 3.15-2.15 (m, 9H), 3.65 (s, 2H, —CH2Ph), 4.46 (m, 1H, —CHF), 4.61 (m, 1H, —CHF), 7.31 (m, 5H, ArH). 13C NMR (CDCl3): δ 18.1, 27.5, 43.8, 53.9, 56.7, 57.5, 60.4, 82.4, 84.6, 126.6, 128.1, 128.5, 139.0. LCMS: m/z calcd for C15H23FN2 ([M]+) 250. found 251 ([M+H]+).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08173636B2 |
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| Source dataset | uspto-grants-2012_05 |
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| ORD ID | ord-8cf8c99137334fc1a7825534423a4666 |
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| Source note | uspto-grants-2012_05 |
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