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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 471876Generated: October 30, 2026

Hydrochloric Acid → N-{[4'-(1H-1,2,4-triazol-3-yl)-3-biphenylyl]methyl}-2,3-dihydro-1H-inden-2-amine hydrochloride

https://huagongshe.com/reaction/471876

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantMethanolHCID 887—
ReactantSodium CarbonateHCID 10340—
ReactantSodium MethoxideHCID 10942334—
ReactantHCID 58276358HCID 58276358—
SolventEthanolHCID 702—
SolventWaterHCID 962—
ProductN-{[4'-(1H-1,2,4-triazol-3-yl)-3-biphenylyl]methyl}-2,3-dihydro-1H-inden-2-amine hydrochlorideHCID 17847820489%

Reaction Steps

To a solution of (3-{3′-[(2,3-dihydro-1H-inden-2-ylamino)methyl]-4-biphenylyl}-1H-1,2,4-triazol-1-yl)methyl 2,2-dimethylpropanoate (0.084 g, 0.17 mmol, Example X-3) in EtOH (1.5 mL) was added a 4.37 M solution of NaOMe in MeOH (0.08 mL, 0.35 mmol). The mixture was stirred for 50 min at RT. A 1.2M solution of concentrated HCl in EtOH was added (1.2 mL), and the mixture was heated at 80° C. for 1 h. The reaction mixture was cooled, diluted with water, and basified to a pH of 10 with addition of saturated Na2CO3 (aq). The mixture was extracted with EtOAc. The combined organic extracts were washed with water and brine, dried with anhydrous Na2SO4, and concentrated in vacuo. The residue was dissolved in CH2Cl2 and MeOH, and 4N HCl in dioxane was added (0.2 mL). After stirring for 15 min, the precipitate was filtered, washed with CH2Cl2, and dried, affording the title compound as a colorless solid (0.057 g, 89%). (M+H) 367, 1.74 min (LC/MS Method B).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08633175B2
Source datasetuspto-grants-2014_01
ORD IDord-7d36806915264b38b7b5808afa1a06e7
Source noteuspto-grants-2014_01