HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1943922Generated: October 26, 2026
Cyclopropanecarboxaldehyde → cyclopropyl(1H-pyrazolo[3,4-b]pyridin-3-yl)methanol
https://huagongshe.com/reaction/1943922
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Cyclopropanecarboxaldehyde | HCID 123114 | — |
| Reactant | HCID 178418918 | HCID 178418918 | — |
| Reactant | HCID 178506575 | HCID 178506575 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Solvent | Ammonium Chloride | HCID 25517 | — |
| Product | cyclopropyl(1H-pyrazolo[3,4-b]pyridin-3-yl)methanol | HCID 178520052 | 45.9% |
Reaction Steps
i-PrMgCl (0.32 mL, 0.64 mmol) was added to 3-iodo-1H-pyrazolo[3,4-b]pyridine (3.1 mL, 0.61 mmol) in THF (3 mL) at 0° C. After 10 minutes, another portion of i-PrMgCl (0.32 mL, 0.64 mmol) was added. After 10 minutes, neat cyclopropanecarbaldehyde (0.074 mL, 0.98 mmol) was added dropwise and stirred at 0° C. for 1 hour. The mixture was diluted with EtOAc (5 mL) and aqueous ammonium chloride, and extracted with EtOAc (2×5 mL). The resulting residue was purified via flash chromatography eluting with EtOAc to afford cyclopropyl(1H-pyrazolo[3,4-b]pyridin-3-yl)methanol (0.052 g, 0.28 mmol, 44.9% yield).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08394795B2 |
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| Source dataset | uspto-grants-2013_03 |
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| ORD ID | ord-305c142aa19f4ebf8afec2d8f46b813d |
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| Source note | uspto-grants-2013_03 |
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