Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1241453Generated: October 31, 2026

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

https://huagongshe.com/reaction/1241453

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 1A) is mixed with 61.25 ml (60.77 g, 0.613 mol) 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 with 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 numberUS07115599B2
Source datasetuspto-grants-2006_10
ORD IDord-2c157b0917094926aff0ab7cecba33c3
Source noteuspto-grants-2006_10