Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Iodoethane | HCID 6340 | — |
| Reactant | Cesium carbonate | HCID 10796 | — |
| Reactant | 4-Bromo-2-isonicotinoylthiophene-3-carboxylic acid | HCID 71743608 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | HCID 89539133 | HCID 89539133 | 90% |
Reaction Steps
A mixture of 4-bromo-2-isonicotinoylthiophene-3-carboxylic acid (311 mg, 1 mmol), ethyl iodide (234 mg, 1.5 mmol), Cs2CO3 (652 mg, 2 mmol) in CH3CN (50 mL) was stirred at 30° C. overnight. After completion of the reaction the solution was filtered and the volatile components removed under reduced pressure to give the title compound (305 mg, 90% yield) as yellow oil. The product was directly used for the next step without further purification. LC-MS (Method A): m/z 340 (M+H)+, Rt: 1.95 min.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09200005B2 |
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| Source dataset | uspto-grants-2015_12 |
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| ORD ID | ord-1c8cfb2b5447441c92502231688daa8a |
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| Source note | uspto-grants-2015_12 |
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