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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 354174Generated: October 31, 2026

Lithium Chloride → 5-(2-Butoxy-5-[2-pyridyl]-3-pyridinyl)-3-ethyl-2-(2-methoxyethyl)-2,6-dihydro-7h-pyrazolo[4,3-d]pyrimidin-7-one

https://huagongshe.com/reaction/354174

Reaction equation

Participants

RoleNameHCIDCharge
ReactantLithium ChlorideHCID 433294—
Reactant5-(2-Butoxy-5-iodo-3-pyridinyl)-3-ethyl-2-(2-methoxyethyl)-2,6-dihydro-7H-pyrazolo[4,3-d]pyrimidin-7-oneHCID 135456031—
CatalystHCID 178418397HCID 178418397—
Solvent1,4-DioxaneHCID 31275—
Product5-(2-Butoxy-5-[2-pyridyl]-3-pyridinyl)-3-ethyl-2-(2-methoxyethyl)-2,6-dihydro-7h-pyrazolo[4,3-d]pyrimidin-7-oneHCID 13573057858%

Reaction Steps

2-Tributyltin pyridine (192 mg, 0.52 mmol), lithium chloride (170 mg, 4.00 mmol), cuprous iodide (11.5 mg, 0.06 mmol), Pd(PPh3)4 (46.5 mg, 0.04 mmol) and the title compound of Example 1 (200 mg, 0.40 mmol) were stirred together in dioxan (10 mL) under a nitrogen atmosphere. The mixture was heated at reflux for 3.5 h, allowed to cool and the solvent removed in vacuo. The residue was taken up in ethyl acetate and shaken vigorously with 5% aqueous potassium fluoride solution for 10 min and the mixture filtered through Arbocel®. The organic layer was separated, washed with 5% aqueous potassium fluoride solution, saturated sodium bicarbonate solution and brine. The organics were dried (MgSO4) and concentrated. The solid was partially purified by trituration with cold ethyl acetate and further purified by flash column chromatography (elution with 50:1 dichloromethane/methanol) to give the title compound (52 mg, 29%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06756373B1
Source datasetuspto-grants-2004_06
ORD IDord-e44a27c4d98f44749fc9b11962c5f8e3
Source noteuspto-grants-2004_06