HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 389588Generated: October 26, 2026
Sodium Hydroxide → HCID 178419486, compound
https://huagongshe.com/reaction/389588
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | Bromine | HCID 24408 | — |
| Reactant | Ammonium Chloride | HCID 25517 | — |
| Reactant | 1H-Pyrazolo[3,4-c]pyridine | HCID 6451441 | — |
| Reactant | HCID 86662424 | HCID 86662424 | — |
| Solvent | Water | HCID 962 | — |
| Product | HCID 178419486 | HCID 178419486 | 62% |
Reaction Steps
To a solution of 1H-pyrazolo[3,4-c]pyridine (0.50 g, 3.5 mmol) in water (10 mL) was added a solution of sodium oxybromide (prepared by dropwise addition of bromine (0.25 mL) to sodium hydroxide solution (0.40 mg in 5 mL) at 0° C. over 5 min). The reaction mixture stirred for 1 h at 10° C. The mixture was then acidified to pH ˜5.5 with ammonium chloride, and extracted with ethyl acetate (3×20 mL). The combined organic fractions were dried over sodium sulfate and concentrated to afford 0.43 g (62%) of the title compound. 1H NMR (300 MHz, CD3OD): δ 7.79 (dd, J=1.5, 4.2 Hz, 1H), 8.32-8.33 (d, J=5.7 Hz, 1H), 9.07 (s, 1H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08378104B2 |
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| Source dataset | uspto-grants-2013_02 |
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| ORD ID | ord-8eaa4b44964b4cc5b106a9d59b9c7fc4 |
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| Source note | uspto-grants-2013_02 |
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