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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2191900Generated: October 30, 2026

Ammonia → methyl 3-[2-allyl-6-(methylthio)-3-oxo-1,2-dihydro-3H-pyrazolo[3,4-d]pyrimidin-1-yl]benzoate

https://huagongshe.com/reaction/2191900

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAmmoniaHCID 222—
ReactantPyridineHCID 1049—
Reactant3-(Methoxycarbonyl)benzeneboronic acidHCID 2734714—
Reactant2-Allyl-6-(methylthio)-1H-pyrazolo[3,4-d]pyrimidin-3(2H)-oneHCID 67171470—
CatalystCupric acetateHCID 8895—
SolventWaterHCID 962—
SolventChloroformHCID 6212—
Productmethyl 3-[2-allyl-6-(methylthio)-3-oxo-1,2-dihydro-3H-pyrazolo[3,4-d]pyrimidin-1-yl]benzoateHCID 6717101555.7%

Reaction Steps

Pyridine (20 mL) was added to a chloroform solution of 2-allyl-6-(methylthio)-1,2-dihydro-3H-pyrazolo[3,4-d]pyrimidin-3-one (7.5 g), copper(II)acetate (6.1 g) and [3-(methoxycarbonyl)]phenylboronic acid (10 g), and stirred at room temperature for 3 days. Aqueous 30% ammonia solution and saturated saline water were added to the reaction liquid in order, and extracted with chloroform. The organic layer was washed with saturated saline water, dried with anhydrous magnesium sulfate, and the solvent was evaporated away. The crude product was purified through silica gel column chromatography (hexane/ethyl acetate) to give methyl 3-[2-allyl-6-(methylthio)-3-oxo-1,2-dihydro-3H-pyrazolo[3,4-d]pyrimidin-1-yl]benzoate as a yellow oil (6.7 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08329711B2
Source datasetuspto-grants-2012_12
ORD IDord-9e64eb403fa743f88c98f4ae86aa30a1
Source noteuspto-grants-2012_12