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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1704767Generated: October 30, 2026

3-(Trifluoromethyl)aniline → 8-Ethyl-N-[3-(trifluoromethyl)phenyl]-8H-pyrazolo[4',3':5,6]pyrido[3,4-e][1,2,4]triazolo[1,5-a]pyrimidin-5-amine

https://huagongshe.com/reaction/1704767

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-(Trifluoromethyl)anilineHCID 7375—
ReactantTriethylamineHCID 8471—
Reactant5-Chloro-8-ethyl-8H-pyrazolo[4',3':5,6]pyrido[3,4-e][1,2,4]-triazolo[1,5-a]pyrimidineHCID 22758486—
Solvent1-ButanolHCID 263—
Product8-Ethyl-N-[3-(trifluoromethyl)phenyl]-8H-pyrazolo[4',3':5,6]pyrido[3,4-e][1,2,4]triazolo[1,5-a]pyrimidin-5-amineHCID 22758504—

Reaction Steps

5.8 g. of 5-chloro-8-ethyl-8H-pyrazolo[4',3':5,6]-pyrido[3,4-e][1,2,4]triazolo[1,5-a]pyrimidine (0.02 mol.), 3 g. of triethylamine and 3.3. g. of 3-trifluoromethylaniline are refluxed in butyl alcohol for 24 hours with stirring. The solvent is removed in vacuo and the residue treated with 20 ml. of water and filtered off. Recrystallization from alcohol yields 8-ethyl-N-[3-(trifluoromethyl)phenyl]-8H-pyrazolo[4',3':5,6]pyrido[3,4-e][1,2,4]triazolo[1,5-a]-pyrimidin-5-amine.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04127655
Source datasetuspto-grants-1978_11
ORD IDord-248966a1a3bd4049bb5bd5ce9299791d
Source noteuspto-grants-1978_11