Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Imidazole | HCID 795 | — |
| Reactant | Iodine | HCID 807 | — |
| Reactant | Nitrogen | HCID 947 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | Triphenylphosphine | HCID 11776 | — |
| Reactant | Pyrrolidine | HCID 31268 | — |
| Reactant | HCID 178523769 | HCID 178523769 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 178511533 | HCID 178511533 | — |
Reaction Steps
In a flame dried round-bottomed flask equipped with a magnetic stir bar and under inert atmosphere (N2), to an ice-cold solution of trans-4-benzyloxycarbonylaminocyclohexane-methanol (292 mg, 1.11 mmol), triphenylphoshine on polystyrene (3.52 mmol) and imidazole (107 mg, 1.55 mmol) in dry CH2Cl2 (40 mL) was added iodine (455 mg, 1.77 mmol). The reaction mixture was warmed to rt and stirred at this temperature until completion of the reaction. The mixture was then filtered, successively washed with 10% aq. Na2SO3 and brine, dried over Na2SO4, filtered and concentrated under reduced pressure. The crude iodide was redissolved in CH3CN (15 mL) and treated with pyrrolidine (0.34 mL, 4.09 mmol) and K2CO3 (566 mg, 4.09 mmol). The reaction mixture was refluxed until completion of the reaction, filtered and concentrated under reduced pressure. The amine was purified by FC (hept-EA, 1:0->1:1) and then the Cbz group was removed by treatment with 10% Pd/C (147 mg) in MeOH (10 mL) under a H2 atmosphere. The title compound was obtained as a colorless oil. LC-MS-conditions 07d: tR=0.97 min; [M+H]+=183.37.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08563714B2 |
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| Source dataset | uspto-grants-2013_10 |
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| ORD ID | ord-d1c492ca251f4f048adf3869a4bdd8db |
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| Source note | uspto-grants-2013_10 |
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