Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1469915Generated: October 27, 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/1469915

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 numberUS09006277B2
Source datasetuspto-grants-2015_04
ORD IDord-e7f2ac9e22df4e459f5af3ab0592dd9b
Source noteuspto-grants-2015_04