Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrogen Bromide | HCID 260 | — |
| Reactant | HCID 68953028 | HCID 68953028 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Product | HCID 54713250 | HCID 54713250 | — |
Reaction Steps
To a solution of N-(4-fluorobenzyl)-3-methoxy-5-methyl-4-oxo-4,5-dihydropyrazolo[1,5-a]quinoxaline-2-carboxamide (85 mg, 0.22 mmol) in AcOH (1 mL) was added 30% HBr in AcOH (2 mL). The mixture was stirred and warmed to 50° C. for 8 hours. The solvent was removed under reduced pressure. The residue was triturated in AcOH to give the title compound as a white solid. 1H NMR (400 MHz, d6-DMSO) δ 9.82 (br s, 1H), 9.06 (t, J=6.0 Hz, 1H), 8.20 (d, J=8.0 Hz, 1H), 7.58 (d, J=7.8 Hz, 1H), 7.51 (t, J=7.8 Hz, 1H), 7.38-7.43 (m, 3H), 7.17 (t, J=9.0 Hz, 2H), 4.50 (d, J=6.2 Hz, 2H), 4.02 (s, 3H), 3.57 (s, 3H); ES MS (M+1)=367.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07476666B2 |
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| Source dataset | uspto-grants-2009_01 |
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| ORD ID | ord-bfaf887605984e6fbcddf9ed24ff3a27 |
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| Source note | uspto-grants-2009_01 |
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