Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 1-Iodopropane | HCID 33643 | — |
| Reactant | HCID 10439236 | HCID 10439236 | — |
| Solvent | Chloroform | HCID 6212 | — |
| Product | HCID 69101078 | HCID 69101078 | — |
Reaction Steps
To 4.9 mg of (2R)-1-{(2S,4R)-4-hydroxy-1-(3,3,3-triphenylpropanoyl)pyrrolidin-2-yl)carbonyl-N-{((3S)-1-propyl-3-piperidyl)methyl}pyrrolidine-2-carboxamide, 1 ml of propyl iodide was added at room temperature, followed by 15 hours' stirring at 100° C. under heating. The reaction liquid was diluted with chloroform, the solvent was distilled off under reduced pressure, and the resulting residue was purified with preparative thin-layer chromatography (aluminium oxide 60F254, Art 5713 (Merck), chloroforom/methanol=18/1) to provide 4.1 mg of the title compound as a pale yellow solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06809108B1 |
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| Source dataset | uspto-grants-2004_10 |
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| ORD ID | ord-cac6244da6d64f7ba7c9f6d48a51bca4 |
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| Source note | uspto-grants-2004_10 |
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