Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrogen Bromide | HCID 260 | — |
| Reactant | HCID 16755043 | HCID 16755043 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Product | HCID 86613285 | HCID 86613285 | — |
Reaction Steps
A solution of 1-(1H-indol-2-yl)-3-(methylthio)imidazo[1,5-a]pyrazin-8-amine (250 mg, 0.85 mmol) in AcOH (10 mL) was treated with 48% hydrogen bromide (0.6 mL) and the mixture heated 120° C. for 24 h. The reaction mixture was then cooled and the suspended solid isolated by filtration and washed with hexane to afford 240 mg of 8-amino-1-(1H-indol-2-yl)imidazo[1,5-a]pyrazine-3(2H)-thione hydrobromide. 1H NMR (400 MHz, MeOD) δ ppm 6.89 (d, J=6.06 Hz, 1H), 7.03 (s, 1H), 7.17 (tt, J=7.07, 0.76 Hz, 1H), 7.31 (tt, J=7.33, 1.01 Hz, 1H), 7.52 (dd, J=0.76 Hz, 1H), 7.63-7.76 (m, 2H); MS (ES+): m/z 282.07 [MH+].
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07648987B2 |
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| Source dataset | uspto-grants-2010_01 |
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| ORD ID | ord-420983ed769d48d095a2f814a139d7e7 |
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| Source note | uspto-grants-2010_01 |
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