Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Cesium carbonate | HCID 10796 | — |
| Reactant | 1,4-Dioxane | HCID 31275 | — |
| Reactant | 2-Thiopheneboronic acid | HCID 2733960 | — |
| Reactant | HCID 58446988 | HCID 58446988 | — |
| Catalyst | HCID 178418397 | HCID 178418397 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Sodium chloride; water | HCID 57417360 | — |
| Product | HCID 58446992 | HCID 58446992 | 70% |
Reaction Steps
A 100 mL round bottom flask was charged with tert-butyl 4-(5-bromo-3-cyanopyrazin-2-yl)piperazine-1-carboxylate (1.0 g, 2.7 mmol), thiophen-2-ylboronic acid (0.52 g, 4.1 mmol), Pd(PPh3)4 (0.31 g, 0.27 mmol), Cs2CO3 (1.4 g, 4.1 mmol), 1,4-dioxane (20 mL) and water (10 mL). The resulting mixture was heated at 100° C. overnight under N2 atmosphere. Work-up: the reaction mixture was poured into brine (80 mL) and extracted with EtOAc (30 mL×3). The combined organic layers were dried over anhydrous Na2SO4 and concentrated in vacuo. The residue was further purified by flash column chromatography on silica gel with 30% EtOAc in petroleum ether, to afford 700 mg (70%) of the product.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US08569300B2 |
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| Source dataset | uspto-grants-2013_10 |
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| ORD ID | ord-9c79e295aef449a08416e741730ef6cb |
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| Source note | uspto-grants-2013_10 |
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