Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 9H-Fluoren-2-yl isocyanate | HCID 4118622 | — |
| Reactant | HCID 58960949 | HCID 58960949 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 11706696 | HCID 11706696 | 44% |
Reaction Steps
To a solution of N-[2-(2-methylbenzothiazol-5-yloxy)-1-(piperazinylmethyl)ethyl]-acetamide (18.4 mg) in tetrahydrofuran (1 ml) was added triethylamine (25.6 μl) and 2-fluorenyl isocyanate (9.5 mg). The reaction mixture was stirred at 55° C. for 4 hours, producing a white precipitate. The precipitate was filtered off, and solvent removed from the filtrate under reduced pressure. The residue was purified by thin layer chromatography, developing with 4% methanol/methylene chloride, to provide N-{2-[4-(N-fluoren-2-ylcarbamoyl)piperazinyl]-1-[(2-methylbenzothiazol-5-yloxy)methyl]ethyl}acetamide (11.2 mg), a compound of Formula I.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07601721B2 |
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| Source dataset | uspto-grants-2009_10 |
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| ORD ID | ord-4b0d3c9bd079434cafa2b586a664c2e8 |
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| Source note | uspto-grants-2009_10 |
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