Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Chloroacetone | HCID 6571 | — |
| Reactant | HCID 62148617 | HCID 62148617 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 67055861 | HCID 67055861 | 66% |
Reaction Steps
To a solution of 2-amino-5-bromo-N-tert-butylpyridine-3-sulfonamide (3.0 g, 9.7 mmol) in ethanol (6 mL) was added chloroacetone (3.0 mL, 48 mmol) and the reaction mixture was stirred at 80° C. for 48 h. The solvents were evaporated under reduced pressure and the residue was purified by flash silica gel column chromatography (5% methanol in DCM) to yield 6-bromo-N-tert-butyl-2-methylimidazo[1,2-a]pyridine-8-sulfonamide (2.2 g, 66%), which was used without further purification. LCMS Method T: retention time 1.33 min; [M+1]=346.64.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08575184B2 |
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| Source dataset | uspto-grants-2013_11 |
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| ORD ID | ord-7a387e572f88485ca3fb25a2df2736da |
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| Source note | uspto-grants-2013_11 |
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