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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2120567Generated: November 1, 2026

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

https://huagongshe.com/reaction/2120567

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 3A) is treated 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, the residue is added to 2 l of water and the mixture is extracted three times with 1 l of ethyl acetate each time. The combined organic phases are dried using magnesium sulphate and concentrated in a rotary evaporator. The residue is chromatographed on 2.5 g of silica gel and eluted with a toluene/toluene-ethyl acetate=4:1 gradient. Yield: 91.6 g (49.9% of theory over two steps).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06693102B2
Source datasetuspto-grants-2004_02
ORD IDord-77311ec7313649e19b71dadc8421b82e
Source noteuspto-grants-2004_02