HuagongsheHuagongshe Chemistry Print Report · For research reference only
Sodium Iodide → 6-(3-Picolinyloxy)-2-cyanobenzothiazole
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Sodium Iodide | HCID 5238 | — |
| Reactant | Cesium carbonate | HCID 10796 | — |
| Reactant | 2-Cyano-6-hydroxybenzothiazole | HCID 9881912 | — |
| Reactant | 3-(Bromomethyl)pyridine hydrobromide | HCID 12707037 | — |
| Solvent | Acetone | HCID 180 | — |
| Product | 6-(3-Picolinyloxy)-2-cyanobenzothiazole | HCID 58427770 | 61% |
Reaction Steps
To a solution of 2-cyano-6-hydroxybenzothiazole (0.39 g, 2.2 mmol) in acetone (50 mL) was added 3-(bromomethyl)pyridine hydrobromide (0.7 g, 2.76 mmol), cesium carbonate (2.15 g, 6.6 mmol), and a catalytic amount of sodium iodide. After adding 3 A molecular sieves, the yellow suspension was refluxed for 40 h under nitrogen. After cooling down the mixture and filtering the solids, the filtrate was concentrated and the residue was purified by silica gel chromatography using 50%-100% ethyl acetate in heptane. A yellowish solid was obtained in 61% yield. MS (ESI+): m/z 267.64 (M+H)+; calc'd: 268.05.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08106052B2 |
| Source dataset | uspto-grants-2012_01 |
| ORD ID | ord-5c49c3cff50f4f038ff947c50c11b54d |
| Source note | uspto-grants-2012_01 |