Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Benzyl Bromide | HCID 7498 | — |
| Reactant | Phenyl isocyanate | HCID 7672 | — |
| Reactant | Piperidine | HCID 8082 | — |
| Reactant | HCID 67004890 | HCID 67004890 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | HCID 53788322 | HCID 53788322 | 44.4% |
Reaction Steps
A solution of (S)-3-[N-{3-(trifluoromethyl)benzoyl}glycyl]aminopyrrolidine (0.060 mmol) in CH3CN (1.1 mL) and (piperidinomethyl)polystyrene (2.6-2.8 mmol/g, 30 mg) were added to a solution of benzyl bromide (0.050 mmol) in CH3CN (0.4 mL). The reaction mixture was stirred at 45° C. for 5 h. After the mixture was cooled to room temperature, the resin was removed by filtration and the filtrate was concentrated. The residue was resolved in CH3CN (1.0 mL) and phenyl isocyanate (0.008 mL, 0.05 mmol) was added. The mixture was stirred at room temperature for 1 h, loaded onto Varian™ SCX column, and washed with CH3OH (15 mL). Product was eluted off using 2 N NH3 in CH3OH (6 mL) and concentrated to afford (S)-1-benzyl-3-[N{3-(trifluoromethyl)benzoyl}glycyl]aminopyrrolidine (compound No.239) (9.0 mg, 44%): The purity was determined by RPLC/MS (99%); ESI/MS m/e 406.0 (M++H, C21H22F3N3O2).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06410566B1 |
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| Source dataset | uspto-grants-2002_06 |
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| ORD ID | ord-48e73d66248945a0b3c776bfb39424fb |
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| Source note | uspto-grants-2002_06 |
|---|