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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1500654Generated: October 26, 2026

Ammonium Chloride → 4-Isopropyl-6-[4-(1-methyl-1H-indol-5-yl)-5-phenylamino-4H-[1,2,4]triazol-3-yl]-benzene-1,3-diol

https://huagongshe.com/reaction/1500654

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAmmonium ChlorideHCID 25517—
ReactantEinecs 211-027-4HCID 69401—
Reactant[5-(5-isopropyl-2,4-dimethoxy-phenyl)-4-(1-methyl-1H-indol-5-yl)-4H-[1,2,4]triazol-3-yl]-phenylamineHCID 59729571—
SolventDichloromethaneHCID 6344—
Product4-Isopropyl-6-[4-(1-methyl-1H-indol-5-yl)-5-phenylamino-4H-[1,2,4]triazol-3-yl]-benzene-1,3-diolHCID 13597186666.7%

Reaction Conditions

Temperature210 °C

Reaction Steps

A flask was charged with [5-(5-Isopropyl-2,4-dimethoxy-phenyl)-4-(1-methyl-1H-indol-5-yl)-4H-[1,2,4]triazol-3-yl]-phenyl-amine (27 mg; 0.06 mmol) and pyridinium chloride (2 g.). The reactants were placed under a nitrogen atmosphere, and the reaction was heated to 210° C. for 25 minutes. To the cooled reaction mixture was added dichloromethane and saturated ammonium chloride solution. The organic fraction was isolated, and the product was purified by column chromatography to give 4-Isopropyl-6-[4-(1-methyl-1H-indol-5-yl)-5-phenylamino-4H-[1,2,4]triazol-3-yl]-benzene-1,3-diol (18 mg; 0.04 mmol.)

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09206162B2
Source datasetuspto-grants-2015_12
ORD IDord-5609e872100945f6b6af4a7188774ac1
Source noteuspto-grants-2015_12