Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Dimethyl Sulfoxide | HCID 679 | — |
| Reactant | HCID 9816454 | HCID 9816454 | — |
| Product | HCID 434493 | HCID 434493 | — |
Reaction Steps
(±)-3-(4-trifluoromethylphenyl)-8-azabicyclo[3.2.1]oct-2-ene in the form of a free amine (1 mg) was dissolved in anhydrous dimethyl sulphoxide (DMSO; 300 ml), and then reacted with [11C]-methyl iodide and heated for 5 min at 130° C. The resulting N-[11C]-methyl labelled [11C]-compound was subsequently purified by HPLC. Removal of the HPLC solvent was achieved by heating the [11C]-labelled (±)8-methyl-3-(4-trifluoromethylphenyl)-8-azabicyclo[3.2.1]oct-2-ene containing fraction under reduced pressure. The labelled product was then formulated in saline or water (10 ml) and passed over a 0.22 mm membrane filter into a sterile vial.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06617459B2 |
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| Source dataset | uspto-grants-2003_09 |
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| ORD ID | ord-7a8156bed9e74a1e908b9c0c449bd12d |
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| Source note | uspto-grants-2003_09 |
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