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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2375022Generated: October 26, 2026

p-Toluenesulfonic acid → 5-methyl-N-[4-(methyloxy)phenyl]-7-phenylimidazo[5,1-f][1,2,4]triazin-2-amine

https://huagongshe.com/reaction/2375022

Reaction equation

Participants

RoleNameHCIDCharge
Reactantp-Toluenesulfonic acidHCID 6101—
ReactantP-AnisidineHCID 7732—
Reactant5-Methyl-2-(methylthio)-7-phenylimidazo[5,1-F][1,2,4]triazineHCID 53471832—
Reactant5-Methyl-2-(methylsulfonyl)-7-phenylimidazo[5,1-F][1,2,4]triazineHCID 53471833—
SolventTetrahydrofuranHCID 8028—
Product5-methyl-N-[4-(methyloxy)phenyl]-7-phenylimidazo[5,1-f][1,2,4]triazin-2-amineHCID 4458972923.2%

Reaction Steps

A mixture of 5-methyl-2-(methylthio)-7-phenylimidazo[5,1-f][1,2,4]triazine (Intermediate 72) (75 mg, 0.26 mmol), p-anisidine (32 mg, 0.26 mmol) and p-toluenesulfonic acid (5 mg, 0.03 mmol) in tetrahydrofuran (5 mL) was stirred at reflux overnight. The mixture was then reduced under vacuum, and purified by chromatography on silica gel eluting with 40% ethyl acetate in petrol to give a solid which was purified further by trituration with diethyl ether to afford 5-methyl-N-[4-(methyloxy)phenyl]-7-phenylimidazo[5,1-f][1,2,4]triazin-2-amine (20 mg) as a yellow solid. MS m/z 332 (M+1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07462614B2
Source datasetuspto-grants-2008_12
ORD IDord-88e2f0a548fc4ef6a869887740058b12
Source noteuspto-grants-2008_12