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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

Reaction equation

Participants

RoleNameHCIDCharge
ReactantCyclopropanecarboxaldehydeHCID 123114—
ReactantHCID 178418918HCID 178418918—
ReactantHCID 178506575HCID 178506575—
SolventTetrahydrofuranHCID 8028—
SolventEthyl AcetateHCID 8857—
SolventAmmonium ChlorideHCID 25517—
Productcyclopropyl(1H-pyrazolo[3,4-b]pyridin-3-yl)methanolHCID 17852005245.9%

Reaction Conditions

Temperature0 °C

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08394795B2
Source datasetuspto-grants-2013_03
ORD IDord-305c142aa19f4ebf8afec2d8f46b813d
Source noteuspto-grants-2013_03