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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1962844Generated: October 30, 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/1962844

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 numberUS08415377B2
Source datasetuspto-grants-2013_04
ORD IDord-eb3a53b0a9024872a7604206187ff688
Source noteuspto-grants-2013_04