Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Dimethylformamide | HCID 6228 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | HCID 14193053 | HCID 14193053 | — |
| Reactant | HCID 18326618 | HCID 18326618 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | HCID 18353389 | HCID 18353389 | — |
Reaction Steps
A suspension of 2-(piperidin-4-yl)-4-fluorobenzonitrile hydrochloride (2.5 g, 10.4 nmmol), 3-bromo-1-tert-butoxycarbonylpropylamine (3.22 g, 13.5 mmol) and triethylamine (3.76 ml, 27 mmol) in DMF (12 ml) was stirred at room temperature for 16 hours. The reaction mixture was diluted with ethyl acetate (200 mL) and washed with saturated bicarbonate solution, water×2 and brine. Dying and solvent evaporation gave after flash chromatography (silica gel, ethyl acetate) gave 3.1 g of 2-[1-(3-tert-butoxycarbonylaminopropyl) piperidin-4-yl]-4-fluorobenzonitrile. This material was dissolved in EtOAc (200 mL), cooled to 0° C. and HCl gas was bubbled into the solution for 15 minutes. The reaction mixture was concentrated at reduced pressure to give the product
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06339090B1 |
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| Source dataset | uspto-grants-2002_01 |
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| ORD ID | ord-f171581747c74a78b222647d3fac5e81 |
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| Source note | uspto-grants-2002_01 |
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