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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1881373Generated: November 1, 2026

Hydrochloric Acid → HCID 178516577, compound

https://huagongshe.com/reaction/1881373

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantHCID 178498574HCID 178498574—
SolventMethanolHCID 887—
ProductHCID 178516577HCID 17851657777%

Reaction Conditions

Temperature50 °C

Reaction Steps

To the intermediate (400 mg, 0.77 mmol) was added degassed 2N—NaOH (0.7 mL, 0.35 mmol) and the reaction mixture was stirred at 110° C. for 2 h. After cooled down to room temperature, the reaction mixture was acidified with 1N—HCl. The white precipitate was filtered and dried to give 5-(4,6-Bis-methoxymethoxy-biphenyl-3-yl)-4-naphthalen-1-yl-4H-[1,2,4]triazole-3-thiol as a white solid (250 mg, 65%). 5-(4,6-Bis-methoxymethoxy-biphenyl-3-yl)-4-naphthalen-1-yl-4H-[1,2,4]triazole-3-thiol (190 mg, 0.38 mmol) was dissolved in MeOH (7 mL) and 6N—HCl (0.5 mL) was added to the solution. The reaction mixture was heated at 50° C. for 2 h. After MeOH was removed under vacuum, the reaction mixture was extracted with EtOAc (20 mL×3). The combined organic layers were washed with water and brine and dried over MgSO4. The purification of the concentrated crude product by column chromatography (MeOH 10% in CH2Cl2) afforded the title product as white solid (120 mg, 77%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08318790B2
Source datasetuspto-grants-2012_11
ORD IDord-5a5eaeae83c944fe9ba8b248de8f7bc1
Source noteuspto-grants-2012_11