Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Cesium carbonate | HCID 10796 | — |
| Reactant | 5-Fluoro-1,3-benzothiazole | HCID 18786167 | — |
| Reactant | HCID 117677347 | HCID 117677347 | — |
| 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 117678052 | HCID 117678052 | — |
Reaction Steps
DMF (4.3 mL) was added to a 125 mL round-bottom flask containing 5-fluorobenzo[d]thiazole (268 mg, 1.749 mmol). Compound 23 (420 mg, 0.874 mmol), Pd(Ph3P)4 (202 mg, 0.175 mmol), Cs2CO3 (1709 mg, 5.25 mmol) and CuI (33.3 mg, 0.175 mmol) were then added. The mixture was degassed placed in an oil bath that was preheated to 100° C. for 1 h. The reaction mixture was cooled to room temperature, diluted with water and ethyl acetate and filtered through celite. The organics were then separated and the water layer was washed with ethyl acetate. The organics were combined, washed with brine (×3), dried over sodium sulfate, filtered, and concentrated. The residue was purified by column chromatography on silica gel, eluting with EtOAc/hexane to give the title compound as a white solid. 1H NMR (CDCl3) δ 10.81-10.78 (m, 1H), 7.79-7.75 (m, 1H), 7.62-7.59 (m, 1H), 7.11-7.07 (m, 1H), 4.41-4.89 (m, 1H), 4.16-4.14 (m, 2H), 3.69-3.44 (m, 2H), 2.00-1.25 (m, 13H), LCMS 3.30 min, 506 (M+H)
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09221809B2 |
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| Source dataset | uspto-grants-2015_12 |
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| ORD ID | ord-925e6b14a4d347b997627ffb634d95f2 |
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| Source note | uspto-grants-2015_12 |
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