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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1591658Generated: November 5, 2026

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

https://huagongshe.com/reaction/1591658

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 21 of water and extracted three times with 11 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 numberUS07291622B2
Source datasetuspto-grants-2007_11
ORD IDord-96e28d8c511a4bfd9a96a66b059ac464
Source noteuspto-grants-2007_11