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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 353431Generated: October 30, 2026

Acetic Acid → 1-(2,6-Dichlorophenyl)-6-(4-hydroxybenzyl)-3-isopropyl-1,5-dihydropyrazolo[3,4-d]pyrimidin-4-one

https://huagongshe.com/reaction/353431

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AcidHCID 176—
ReactantEthyl 4-hydroxyphenylacetateHCID 28310—
ReactantSodium ethoxideHCID 2723922—
Reactant5-amino-1-(2,6-dichlorophenyl)-3-isopropyl-1H-pyrazole-4-carboxylic acid amideHCID 18540666—
SolventEthanolHCID 702—
Product1-(2,6-Dichlorophenyl)-6-(4-hydroxybenzyl)-3-isopropyl-1,5-dihydropyrazolo[3,4-d]pyrimidin-4-oneHCID 13573064776%

Reaction Steps

To a suspension of 5-amino-1-(2,6-dichlorophenyl)-3-isopropyl-1H-pyrazole-4-carboxylic acid amide (5.0 g, 16 mmol) in EtOH (20 mL) was added ethyl 4-hydroxyphenylacetate (8.6 g, 48 mmol) followed by NaOEt (2.66M in EtOH, 36 mL, 96 mmol). The reaction was then heated to reflux for 3 h. The reaction was then cooled to room temp and poured onto 10% aq. HOAc (100 mL). The resulting suspension was then cooled to 0° C. and filtered. The precipitate was then washed with 1:1 MeOH/H2O (100 mL) and 1:1 Et2O/hexane (75 mL). The solid was then dried under vacuum to yield the desired product (5.2 g, 76%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06753329B2
Source datasetuspto-grants-2004_06
ORD IDord-e157c286981c4186b12879a5302bdf9a
Source noteuspto-grants-2004_06