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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 393906Generated: October 26, 2026

Benzenesulfonic Acid → 5-(5-Acetyl-2-butoxy-3-pyridinyl)-3-ethyl-2-(1-ethyl-3-azetidinyl)-2,6-dihydro-7H-pyrazolo[4,3-d]pyrimidin-7-one benzenesulfonate

https://huagongshe.com/reaction/393906

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzenesulfonic AcidHCID 7371—
Reactant5-(5-acetyl-2-butoxy-3-pyridinyl)-3-ethyl-2-(1-ethyl-3-azetidinyl)-2,6-dihydro-7H-pyrazolo(4,3-d)pyrimidin-7-oneHCID 135515565—
SolventEthyl AcetateHCID 8857—
Product5-(5-Acetyl-2-butoxy-3-pyridinyl)-3-ethyl-2-(1-ethyl-3-azetidinyl)-2,6-dihydro-7H-pyrazolo[4,3-d]pyrimidin-7-one benzenesulfonateHCID 13567397074.6%

Reaction Conditions

Temperature50 °C

Reaction Steps

5-(5-Acetyl-2-butoxy-3-pyridinyl)-3-ethyl-2-(1-ethyl-3-azetidinyl)-2,6-dihydro-7H-pyrazolo[4,3-d]pyrimidin-7-one (88 mg, 0.2 mmol) was dissolved in warm ethyl acetate (2 mL). A solution of benzenesulfonic acid (32 mg, 0.2 mmol) in ethyl acetate (2 ml) was then added, giving a precipitate. This mixture was warmed to 50° C. for 15 minutes, then allowed to cool to 0° C. The resulting solid was filtered, washed with ethyl acetate and dried in vacuo, to afford the title compound as a white solid 89 mg (74%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06809200B2
Source datasetuspto-grants-2004_10
ORD IDord-687399ae7d49421ab99a133dc87b24eb
Source noteuspto-grants-2004_10