Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | N-bromobutanimide | HCID 67184 | — |
| Reactant | Ethyl 4-ethoxy-1-ethyl-1H-pyrazolo[3,4-b]pyridine-5-carboxylate | HCID 13072976 | — |
| Solvent | Carbon Tetrachloride | HCID 5943 | — |
| Product | CID 14590535 | HCID 14590535 | 50.3% |
Reaction Steps
A mixture of Intermediate 35 (1.0 g, 3.8 mmol) and N-bromosuccinimide (1.49 g, 8.4 mmol) in carbon tetrachloride (35 ml) was heated at reflux for 3 hours. The reaction mixture was cooled in an ice-bath and the precipitate filtered. The filtrate was concentrated in vacuo and the residue dissolved in tetrahydrofuran (12.5 ml). Water (3.5 ml) and saturated sodium carbonate solution (3 ml) were added and the mixture stirred at 20° C. for 18 hours. The reaction was diluted with water and extracted with ethyl acetate. The combined organic phases were dried Na2SO4) and evaporated in vacuo. The residue was purified on an SPE cartridge (silica, 20 g) eluting with dichloromethane, chloroform, then chloroform:methanol (99:1, 49:1, 19:1 then 9:1). Appropriate fractions were combined and evaporated in vacuo to afford Intermediate 36 as an off-white solid (0.45 g). LCMS showed MH++236, TRET=2.46 min.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07528148B2 |
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| Source dataset | uspto-grants-2009_05 |
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| ORD ID | ord-0bfa5079a52f4029a6e3aa97174d01d0 |
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| Source note | uspto-grants-2009_05 |
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