HuagongsheHuagongshe Chemistry Print Report · For research reference only
Water → BOC-4-((S)-2-Methyl-pyrrolidin-1-yl)piperidine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | (2S)-2-methylpyrrolidine | HCID 6999702 | — |
| Reactant | 1-(tert-Butoxycarbonyl)-4-(p-toluenesulfonyloxy)piperidine | HCID 15734713 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | BOC-4-((S)-2-Methyl-pyrrolidin-1-yl)piperidine | HCID 58468064 | 40% |
Reaction Steps
A solution of 4-(toluene-4-sulfonyloxy)-piperidine-1-carboxylic acid tert-butyl ester (8.1 g, 22.8 mmol), (S)-(+)-2-methylpyrrolidine (2.33 g, 27.36 mmol), K2CO3 (6.93 g, 50.16 mmol) in acetonitrile (76 mL) was heated to 80° C. for 20 h and then added additional (S)-(+)-2-methylpyrrolidine (834 mg, 9.79 mmol), and continued heating for 20 h. The heating was removed and the solution was concentrated to provide a residue which was taken up with H2O (100 mL) and extracted with CH2Cl2 (2×100 mL). The organic layer was dried over K2CO3, filtered and concentrated to provide a crude oil which was purified by flash column chromatography (0 to 5% MeOH/CH2Cl2) to provide 2.43 g (40% yield) of the title compound as a solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08859588B2 |
| Source dataset | uspto-grants-2014_10 |
| ORD ID | ord-11c5ffdad5ac4b95a1b091b37cb1dc9f |
| Source note | uspto-grants-2014_10 |