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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1501541Generated: November 1, 2026

2-Bromopropane → ethyl 6-bromo-1-isopropyl-1H-pyrazolo[3,4-b]pyridine-4-carboxylate

https://huagongshe.com/reaction/1501541

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-BromopropaneHCID 6358—
ReactantPotassium CarbonateHCID 11430—
Reactantethyl 6-bromo-1H-pyrazolo[3,4-b]pyridine-4-carboxylateHCID 59766670—
SolventAcetonitrileHCID 6342—
Productethyl 6-bromo-1-isopropyl-1H-pyrazolo[3,4-b]pyridine-4-carboxylateHCID 8670340858.3%

Reaction Steps

To a stirred solution of ethyl 6-bromo-1H-pyrazolo[3,4-b]pyridine-4-carboxylate (20 g, 74.3 mmol) in acetonitrile (200 mL), K2CO3 (15.39 g, 111.52 mmol) and 2-bromopropane (18.13 g, 148.64 mmol) was added to it. The reaction mixture was refluxed for 8 h. On completion, acetonitrile was removed under reduced pressure and water was added to it. Extraction was carried out using ethyl acetate; the combined organic layers were washed with water, brine and dried over anhydrous Na2SO4. Solvent was removed under reduced pressure and residue was purified by silica gel column chromatography to obtain the desired intermediate (13.5 g, 58.3%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09206157B2
Source datasetuspto-grants-2015_12
ORD IDord-9dbca0ad4bbe4769ab276db67eca752b
Source noteuspto-grants-2015_12