HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1992435Generated: October 31, 2026
Dimethyl Sulfoxide → 3-(4-Bromo-phenylsulfanyl)-1-(8-fluoro-2-phenyl-quinolin-7-yl)-imidazo[1,5-a]pyrazin-8-ylamine
https://huagongshe.com/reaction/1992435
Participants
| Role | Name | HCID | Charge |
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| Reactant | Dimethyl Sulfoxide | HCID 679 | — |
| Reactant | Benzenediazonium, 4-bromo-, tetrafluoroborate(1-) (1:1) | HCID 2734810 | — |
| Reactant | 8-Amino-1-(8-fluoro-2-phenyl-quinolin-7-yl)-imidazo[1,5-a]pyrazine-3-thiol | HCID 16753680 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 3-(4-Bromo-phenylsulfanyl)-1-(8-fluoro-2-phenyl-quinolin-7-yl)-imidazo[1,5-a]pyrazin-8-ylamine | HCID 16753679 | — |
Reaction Steps
Into a round bottom flask was added 8-amino-1-(8-fluoro-2-phenyl-quinolin-7-yl)-2H-imidazo[1,5-a]pyrazine-3-thione (21 mg, 0.000053 mol), 4-bromobenzenediazonium tetrafluoroborate (0.018 g, 0.000064 mol) and dimethyl sulfoxide (0.1 mL, 0.002 mol) and the reaction mixture was stirred in ice for 30 min. The reaction mixture was cooled, dissolved in DCM and washed with water. Purification by Gilson HPLC eluting with 10→90% acetonitrile: H2O afforded the title compound as a yellow solid. 1H NMR (400 MHz, CDCl3): δ=7.13-7.17 (m, 2H), 7.23 (d, J=5.05 Hz, 1H), 7.42 (d, J=8.59 Hz, 2H), 7.49-7.59 (m, 3H), 7.61 (d, J=5.05 Hz, 1H), 7.75-7.78 (m, 2H), 8.05 (d, J=8.59 Hz, 1H), 8.22-8.27 (m, 2H), 8.32 (dd, J=8.72, 1.39 Hz, 1H). MS (ES+): m/z 544.15 (100)[MH+]. HPLC: tR=2.69 min (Open Lynx polar—5 min).
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-6f75fc8ef95841bb8ed91d0cb34d7214 |
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| Source note | uspto-grants-2010_01 |
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