HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 38101Generated: October 29, 2026
Boron tribromide → 3-(7-Pyridin-4-yl-pyrazolo[5,1-b]thiazol-6-yl)-phenol
https://huagongshe.com/reaction/38101
Participants
| Role | Name | HCID | Charge |
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| Reactant | Boron tribromide | HCID 25134 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | 6-(3-Methoxy-phenyl)-7-pyridin-4-yl-pyrazolo[5,1-b]thiazole | HCID 67423436 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 3-(7-Pyridin-4-yl-pyrazolo[5,1-b]thiazol-6-yl)-phenol | HCID 46701974 | 80.4% |
Reaction Steps
6-(3-Methoxy-phenyl)-7-pyridin-4-yl-pyrazolo[5,1-b]thiazole (65 mg, 0.212 mmol) was dissolved in dry DCM (2 mL) and cooled to 0° C. A 1 M solution of boron tribromide in DCM (0.850 mL, 0.848 mmol, 4 eq) was added dropwise and the mixture was allowed to warm to room temperature and stirred for 1 hours. Ice was then added to the reaction mixture, followed by saturated aqueous NaHCO3 until pH 6. The aqueous phase was extracted with DCM and the organic layer was dried and evaporated to dryness. An insoluble solid formed during extraction and it was filtered and combined with the organic layer. The crude product was taken up with toluene and concentrated to dryness three times and the same treatment was repeated with DCM. 50 mg of 3-(7-pyridin-4-yl-pyrazolo[5,1-b]thiazol-6-yl)-phenol (80%) were obtained as pale yellow solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08524707B2 |
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| Source dataset | uspto-grants-2013_09 |
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| ORD ID | ord-09b308db305d4ac3808ac399b8414822 |
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| Source note | uspto-grants-2013_09 |
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