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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 81411Generated: October 31, 2026

Trifluoroacetic acid → HCID 136339895, compound

https://huagongshe.com/reaction/81411

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrifluoroacetic acidHCID 6422—
ReactantTrifluoromethanesulfonic acidHCID 62406—
ReactantHCID 68507378HCID 68507378—
SolventDichloromethaneHCID 6344—
ProductHCID 136339895HCID 136339895—

Reaction Steps

To a solution of 2-(biphenyl-4-ylmethyl)-7-(4-methoxybenzyl)-5-methyl-2H-pyrazolo[3,4-d]pyrimidine-4,6(5H,7H)-dione in CH2Cl2 (90 mL) is added TFA (10 mL) slowly at room temperature, followed by adding trifluoromethanesulfonic acid (4 mL) dropwise. After the reaction mixture is stirred at r.t. for 3 hours, solvent is removed under reduced pressure, and the obtained residue is basified by adding cold pre-diluted ammonium hydroxide (NH3 content, 7%) at 0° C. The mixture is extracted with ethyl acetate four times. The combined organic phase is washed with brine, dried over anhydrous Na2SO4, and then filtered. The filtrate is evaporated to dryness to give crude product in almost quantitative yield. MS (ESI) m/z 333.1 [M+H]+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08846693B2
Source datasetuspto-grants-2014_09
ORD IDord-eba80dccf1a642aa855391726adce802
Source noteuspto-grants-2014_09