Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Acetic Acid | HCID 176 | — |
| Reactant | tert-butyl N-methyl-N-(2-oxoethyl)carbamate | HCID 10725881 | — |
| Reactant | HCID 67367332 | HCID 67367332 | — |
| Reactant | CID 101953985 | HCID 101953985 | — |
| Solvent | Methanol | HCID 887 | — |
| Solvent | Chloroform methanol | HCID 21584188 | — |
| Product | HCID 68408166 | HCID 68408166 | 89.4% |
Reaction Steps
7 g (1 eq) 4-phenyl-4-(pyrrolidin-1-yl)piperidine bishydrochloride were added to a solution of 4.4 g (1.1 eq) tert-butyl-methyl(2-oxoethyl)carbamate in 70 ml methanol under a nitrogen atmosphere and the reaction mixture was stirred for 10 min at 0° C. 3.62 g (2.5 eq) sodium cyanoboron hydride were then added and the mixture was stirred for 30 min at room temperature. The reaction mixture obtained was adjusted to a pH of 5-6 with acetic acid and stirred for 14 h at room temperature. The reaction course was monitored by thin-layer chromatography (10% MeOH/CHCl3). Once the conversion was complete, the methanol was distilled off, saturated NaHCO3 solution was added and the mixture obtained was extracted with chloroform (3×50 ml) and the combined organic phases were dried over Na2SO4. Following removal of the solvent under reduced pressure, the residue was purified by column chromatography (silica gel; 50% EtOAc/heptane). 8 g (89%) of product were obtained in the form of a red oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09206156B2 |
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| Source dataset | uspto-grants-2015_12 |
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| ORD ID | ord-a1913d7baf5948c68cae26eed81e746a |
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| Source note | uspto-grants-2015_12 |
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