HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 341236Generated: October 31, 2026
N-Iodosuccinimide → 6-(4-Fluoro-phenyl)-3-iodo-pyrazolo[1,5-a]pyrazine
https://huagongshe.com/reaction/341236
Participants
| Role | Name | HCID | Charge |
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| Reactant | N-Iodosuccinimide | HCID 120273 | — |
| Reactant | 6-(4-Fluoro-phenyl)-pyrazolo[1,5-a]pyrazine | HCID 59321105 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 6-(4-Fluoro-phenyl)-3-iodo-pyrazolo[1,5-a]pyrazine | HCID 59320978 | 76.7% |
Reaction Steps
N-iodosuccinimide (13 mg, 0.06 mmol) was added in one portion to a stirred solution of 6-(4-fluoro-phenyl)-pyrazolo[1,5-a]pyrazine (11 mg, 0.05 mmol) in dry DMF (0.5 ml) at RT under N2. After 30 minutes, a further portion of N-iodosuccinimide (13 mg, 0.06 mmol) in DMF (0.2 mmol) was added. After a further 30 minutes at RT the mixture was heated to 50° C. for 90 minutes. After cooling to RT, the reaction was quenched with saturated aqueous sodium thiosulphate/saturated NaHCO3 (1:1, 1 ml). The mixture was stirred at RT for 1 hour then partitioned between CH2Cl2/H2O. The mixture was passed through a phase separating cartridge. The organic layer was evaporated to give the title compound (13 mg, solid). 1H NMR (400 MHz, CDCl3): 9.01 (1H, d), 8.69 (1H, d), 8.05 (1H, s), 8.00-7.90 (2H, m), 7.24-7.14 (2H, m).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08895745B2 |
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| Source dataset | uspto-grants-2014_11 |
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| ORD ID | ord-b8bd3874d919435cafd8403dfcd14ec5 |
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| Source note | uspto-grants-2014_11 |
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