HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 383562Generated: November 2, 2026
Lithium Hydroxide → HCID 136352699, compound
https://huagongshe.com/reaction/383562
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Lithium Hydroxide | HCID 3939 | — |
| Reactant | N-bromobutanimide | HCID 67184 | — |
| Reactant | HCID 178470166 | HCID 178470166 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | HCID 136352699 | HCID 136352699 | 100% |
Reaction Steps
To a mixture of ethyl 1-(2,6-difluorophenyl)-6-hydroxy-1H-pyrazolo[3,4-b]pyrazine-5-carboxylate (1.27 g, 3.70 mmol) in 2.5 mL of water and 2.5 mL of CH3CN at RT was added lithium hydroxide (209 mg, 8.72 mmol), and the resulting mixture was warmed to 60° C. for 0.5 h. The reaction mixture was cooled with an ice bath, and NBS (1059 mg, 5.95 mmol) was added in small portions. The reaction mixture was stirred at RT for 0.5 h, then partitioned between a saturated solution of NaHCO3 and EtOAc. The EtOAc layer was washed with brine, dried over MgSO4, filtered and concentrated to afford 5-bromo-1-(2,6-difluorophenyl)-1H-pyrazolo[4,3-b]pyrazin-6(7H)-one (1210 mg, 93.3% yield) a a brown amorphous solid. This crude material was used without further purification. MS (ES+): 327.0/329.0 (M+H)+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08367671B2 |
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| Source dataset | uspto-grants-2013_02 |
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| ORD ID | ord-95e6f78ebff74c7f974840f9da8e10d3 |
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| Source note | uspto-grants-2013_02 |
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