Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 3-Bromothiophene | HCID 13383 | — |
| Reactant | Ammonium Chloride | HCID 25517 | — |
| Reactant | HCID 10958318 | HCID 10958318 | — |
| Reactant | HCID 178418306 | HCID 178418306 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 18518623 | HCID 18518623 | 99% |
Reaction Steps
To 3-bromothiophene (105.5 mg, 2.1 eq) in anhydrous THF (2 mL) under a nitrogen atmosphere and with stirring was added t-BuLi (0.38 mL, 2.1 eq, 1.7 M in pentane) at −40° C. (bath temperature). Stirring was continued for 30 minutes after which 1-(2-diethylaminoethyl)-4-bromoisatin (100.0 mg, 3.08×10−4 mol) in anhydrous THF (2 mL) was added dropwise. The resulting red colored solution was stirred at −40° C. for 8 hours. Saturated aqueous NH4Cl (1.5 mL) was added and the reaction mixture was allowed to warm to room temperature. The mixture was extracted with EtOAc and the combined extracts were dried (anhydrous Na2SO4). After filtration the solvent was removed in vacuo. Purification was carried out by column chromatography (silica gel, eluting 1% to 2% MeOH in CHCl3) to give the title compound as a light brown foam (124.5 mg, 99%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06576656B1 |
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| Source dataset | uspto-grants-2003_06 |
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| ORD ID | ord-31549d43439545a9baed87308b301e8c |
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| Source note | uspto-grants-2003_06 |
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