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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2205309Generated: November 1, 2026

Hydrochloric Acid → 4-[(1S)-1-[[(3R)-2-(2-(4-fluorophenoxy)ethyl)-3,4-dihydro-1H-isoquinoline-3-carbonyl]amino]ethyl]benzoic acid hydrochloride

https://huagongshe.com/reaction/2205309

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantSodium HydroxideHCID 14798—
Reactant1,4-DioxaneHCID 31275—
Reactantmethyl 4-[(1S)-1-[[(3R)-2-(2-(4-fluorophenoxy)ethyl)-3,4-dihydro-1H-isoquinoline-3-carbonyl]amino]ethyl]benzoateHCID 118876972—
SolventMethanolHCID 887—
SolventTetrahydrofuranHCID 8028—
Product4-[(1S)-1-[[(3R)-2-(2-(4-fluorophenoxy)ethyl)-3,4-dihydro-1H-isoquinoline-3-carbonyl]amino]ethyl]benzoic acid hydrochlorideHCID 8628067393%

Reaction Steps

Dissolve methyl 4-[(1S)-1-[[(3R)-2-(2-(4-fluorophenoxy)ethyl)-3,4-dihydro-1H-isoquinoline-3-carbonyl]amino]ethyl]benzoate (550 mg, 1.15 mmol) in a mixture of methanol (10 mL) and tetrahydrofuran (10 mL). Add a 5 N aqueous solution of sodium hydroxide (0.462 mL, 2.31 mmol), then stir the mixture at room temperature overnight. Concentrate the mixture under reduced pressure to furnish a white solid. Add a 4 M solution of hydrogen chloride in 1,4-dioxane (10 mL, 40 mmol), and stir the mixture at room temperature for 10 min Remove the suspended solids by filtration, rinsing the solids with THF (5 mL). Concentrate the combine filtrate under reduced pressure to furnish a white solid. Triturate the material in hot diethyl ether (10 mL), and filter to furnish the title compound as a white solid (535 mg, 93% yield). Mass spectrum (m/z): 463 ([M+H]+), 485 ([M+Na]+).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09371289B2
Source datasetuspto-grants-2016_06
ORD IDord-b74afaf792bb4e34b3acec080c4986a3
Source noteuspto-grants-2016_06