Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Piperidine | HCID 8082 | — |
| Reactant | HCID 66939751 | HCID 66939751 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 57907460 | HCID 57907460 | — |
Reaction Steps
To a stirred solution of 3.15 g (4.65 mmol) of tert-butyl (2S,5R)-2-{4-[((25)-2-{[(9H-fluoren-9-yloxy)carbonyl]amino}propanoyl)amino]benzyl}-5-[(R)-hydroxy(phenyl)methyl]pyrrolidine-1-carboxylate from step A above in 3 mL of anhydrous THF was added 0.396 g (4.65 mmol) of piperidine. The resulting mixture was heated to 35° C. under an atmosphere of nitrogen for 2 h then all volatiles were removed in vacuo to afford the crude title compound which was used without further purification. LC-MS: m/z (ES) 454 (MH)+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08653260B2 |
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| Source dataset | uspto-grants-2014_02 |
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| ORD ID | ord-7369aea408ee44c1b87ab2422bbcef48 |
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| Source note | uspto-grants-2014_02 |
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