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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2212956Generated: November 1, 2026

Trifluoroacetic acid → 3-Ethoxycarbonyl-1-(2-fluorbenzyl)-1H-pyrazolo-(3,4,5)-pyridin

https://huagongshe.com/reaction/2212956

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrifluoroacetic acidHCID 6422—
ReactantN,N-DimethylacrylamideHCID 17587—
Reactantethyl 5-amino-1-(2-fluorobenzyl)-1H-pyrazole-3-carboxylateHCID 11391384—
Product3-Ethoxycarbonyl-1-(2-fluorbenzyl)-1H-pyrazolo-(3,4,5)-pyridinHCID 11162345—

Reaction Steps

The solution obtained from 2A) is mixed with 61.25 ml (60.77 g, 0.613 mmol) of dimethylaminoacrolein and 56.28 ml (83.88 g, 0.736 mol) of trifluoroacetic acid and boiled under argon for 3 days. The solvent is then evaporated in vacuo, and the residue is added to 2 l of water and extracted three times with 1 l of ethyl acetate each time. The combined organic phases are dried over magnesium sulfate and concentrated in a rotary evaporator. Chromatography is carried out on 2.5 kg of silica gel, eluting with a toluene/toluene-ethyl acetate=4:1 gradient. Yield: 91.6 g (49.9% of theory over two stages).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07105523B2
Source datasetuspto-grants-2006_09
ORD IDord-69fe3f9a36c74fe6bc4a4bbdc28675d6
Source noteuspto-grants-2006_09