Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ammonium Chloride | HCID 25517 | — |
| Reactant | 7-Chlorothieno[3,2-b]pyridine | HCID 11275251 | — |
| Reactant | Potassium tert-butoxide | HCID 23665647 | — |
| Reactant | HCID 66995289 | HCID 66995289 | — |
| Solvent | Dimethyl Sulfoxide | HCID 679 | — |
| Product | HCID 57742595 | HCID 57742595 | 95.1% |
Reaction Steps
A 250 mL flask was charged with tert-butyl 4-(5-(5-(3-methoxy-3-oxopropylthio)-3-phenoxypyridin-2-ylamino)-1,2,4-thiadiazol-3-yl)piperidine-1-carboxylate (10 g, 17 mmol), 7-chlorothieno[3,2-b]pyridine (3.6 g, 21 mmol), and DMSO (125 mL). Nitrogen was bubbled vigorously through the solution for 10 minutes. Potassium 2-methylpropan-2-olate (5.9 g, 52 mmol) was added and the reaction was stirred at ambient temperature under nitrogen for 5 hours. The reaction was poured into saturated aqueous NH4Cl and extracted with EtOAc (1×500 mL). The organic layer was washed with water and brine, dried with sodium sulfate, filtered and concentrated in vacuo. The residue was purified on silica (50 to 75% EtOAc in hexanes) to afford tert-butyl 4-(5-(3-phenoxy-5-(thieno[3,2-b]pyridin-7-ylthio)pyridin-2-ylamino)-1,2,4-thiadiazol-3-yl)piperidine-1-carboxylate (10 g, 92% yield) as a white foam.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08362037B2 |
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| Source dataset | uspto-grants-2013_01 |
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| ORD ID | ord-219e5191ba654aa7a786cae6828eaf51 |
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| Source note | uspto-grants-2013_01 |
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