Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 2-Bromothiazole | HCID 76430 | — |
| Reactant | HCID 67960651 | HCID 67960651 | — |
| Catalyst | Copper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI) | HCID 24350 | — |
| Catalyst | HCID 178418397 | HCID 178418397 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 67959986 | HCID 67959986 | 22.2% |
Reaction Steps
A solution of 2-bromothiazole (20 mg, 0.12 mmol) and benzyl trans-4-fluoro-3-((4-((4-methoxybenzyl)oxy)-6-(1-(tetrahydro-2H-pyran-2-yl)-5-(trimethylstannyl)-1H-indazol-3-yl)pyrimidin-2-yl)oxy)piperidine-1-carboxylate (racemic) (100 mg, 0.12 mmol) in DMF (1 mL) was bubbled with argon for 15 min. To the above mixture was added CuI (11 mg, 0.060 mmol) and Pd(PPh3)4 (13 mg, 0.012 mmol) and argon gas was bubbled for another 15 min. The reaction was heated at 100 C for 2 h. The reaction was quenched with water and the suspension was filtered. The solid was dried then purified with basic alumina chromatography (eluting with 30% EtOAc in hexanes) to give benzyl trans-4-fluoro-3-((4-((4-methoxybenzyl)oxy)-6-(1-(tetrahydro-2H-pyran-2-yl)-5-(thiazol-2-yl)-1H-indazol-3-yl)pyrimidin-2-yl)oxy)piperidine-1-carboxylate (racemic) (20 mg, 11%) as a off brown solid. MS (ESI, pos. ion) m/z: 750.8 (M+1).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09090593B2 |
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| Source dataset | uspto-grants-2015_07 |
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| ORD ID | ord-dbe6c488827646ee85f766bf0cb09eac |
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| Source note | uspto-grants-2015_07 |
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