HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 449008Generated: October 30, 2026
N-Iodosuccinimide → 8-Chloro-1-iodo-3-methylsulfanyl-imidazo[1,5-a]pyrazine
https://huagongshe.com/reaction/449008
Participants
| Role | Name | HCID | Charge |
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| Reactant | N-Iodosuccinimide | HCID 120273 | — |
| Reactant | 8-Chloro-3-(methylsulfanyl)imidazo[1,5-A]pyrazine | HCID 59130382 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | 8-Chloro-1-iodo-3-methylsulfanyl-imidazo[1,5-a]pyrazine | HCID 58901987 | 94% |
Reaction Steps
P To a solution of 8-chloro-3-methylsulfanyl-imidazo[1,5-a]pyrazine (1.75 g, 0.00876 mol) in DMF (15 mL) was added N-iodosuccinimide (3.94 g, 0.0175 mol), the resulting mixture was stirred at 55° C. for 6 hrs. The mixture was diluted with EtOAc (200 mL), washed with sat. aq. NaHCO3 (40 mL), water (2×40 mL), brine (40 mL), and dried over anhydrous sodium sulfate. The crude material was purified by silica gel chromatography to give the title compound as a yellow solid, 2.68 g, 94% yield. 1H NMR (CDCl3, 400 MHz): δ 2.72 (s, 3H), 7.36 (d, J=4.8 Hz, 1H), 7.76 (d, J=4.8 Hz, 1H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08481733B2 |
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| Source dataset | uspto-grants-2013_07 |
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| ORD ID | ord-87439b1cffb448068234f536f9a05e83 |
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| Source note | uspto-grants-2013_07 |
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