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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1501530Generated: November 2, 2026

Bromocyclopentane → HCID 86703404, compound

https://huagongshe.com/reaction/1501530

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBromocyclopentaneHCID 8728—
ReactantPotassium CarbonateHCID 11430—
Reactantethyl 6-bromo-1H-pyrazolo[3,4-b]pyridine-4-carboxylateHCID 59766670—
SolventAcetonitrileHCID 6342—
ProductHCID 86703404HCID 8670340450%

Reaction Steps

Ethyl 6-bromo-1H-pyrazolo[3,4-b]pyridine-4-carboxylate (3 g, 11.15 mmol) was dissolved in acetonitrile (30 mL) and K2CO3 (1.85 g, 13.38 mmol) and cyclopentyl bromide (3.35 g, 22.30 mmol) was added to it. The reaction mixture was refluxed for 3 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 (1.3 g, 50%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09206157B2
Source datasetuspto-grants-2015_12
ORD IDord-32f95b6150b4475683c525be2fea835c
Source noteuspto-grants-2015_12