Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1860572Generated: November 4, 2026

Sodium ethoxide → HCID 178440265, compound

https://huagongshe.com/reaction/1860572

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium ethoxideHCID 2723922—
Reactant5-Amino-3-isopropyl-1-(2,4,6-trichlorophenyl)pyrazole-4-carboxamideHCID 18540630—
ReactantEthyl 3-aminoindazol-5-ylacetateHCID 18540672—
SolventEthanolHCID 702—
ProductHCID 178440265HCID 178440265—

Reaction Steps

To a stirred solution of 139 mg (0.40 mmol) of 5-amino-3-isopropyl-1-(2,4,6-trichlorophenyl)pyrazole-4-carboxamide in 3 mL of absolute ethanol was added 329 mg (1.50 mmol) of ethyl 3-aminoindazol-5-ylacetate followed by 1.13 mL (3.0 mmol) of 2.66 M sodium ethoxide in ethanol. The solution was stirred 16 h at reflux, and the heating mantle was then removed. The reaction was treated with 8 mL of 10% aq. HOAc, poured into water, and extracted with EtOAc. The organic extract was washed with brine, dried (MgSO4), concentrated under reduced pressure, and chromatographed on silica gel (gradient elution with 5% to 10% MeOH—CH2Cl2) to give, after removal of solvent, 123 mg (61%) of 1-(2,4,6-trichlorophenyl)-3-isopropyl-6-(3-aminoindazol-5-ylmethyl)pyrazolo[3,4-d]pyrimidin-4-one as a white, amorphous solid. Mass spec.: 502.0712 (M+H)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06531477B1
Source datasetuspto-grants-2003_03
ORD IDord-b0e726281b794c7d91327139985e7fc5
Source noteuspto-grants-2003_03