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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 508065Generated: November 2, 2026

Hydrochloric Acid → HCID 86624380, compound

https://huagongshe.com/reaction/508065

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantMethanolHCID 887—
ReactantBenzenesulfonic AcidHCID 7371—
ReactantSodium HydroxideHCID 14798—
ReactantHCID 23157691HCID 23157691—
SolventTetrahydrofuranHCID 8028—
SolventEthyl AcetateHCID 8857—
ProductHCID 86624380HCID 8662438056%

Reaction Steps

To a mixture of ethyl 3-{4-[({2′,6′-dimethyl-4′-[3-(2-oxopyrrolidin-1-yl)propoxy]biphenyl-3-yl}methyl)amino]-2-fluorophenyl}propanoate (1.13 g, 2.07 mmol), methanol (5 mL) and tetrahydrofuran (10 mL) was added 1 M aqueous sodium hydroxide solution (4.14 mL), and the mixture was stirred at room temperature for 2 hr. The reaction mixture was neutralized with 1M hydrochloric acid, and diluted with ethyl acetate, and the organic layer was washed with saturated brine, dried, and concentrated under reduced pressure. The residue was purified by silica gel column chromatography (hexane/ethyl acetate=4/1-hexane/ethyl acetate=1/2) to give a colorless oil. The obtained oil was diluted with ethyl acetate, and benzenesulfonic acid was added. The precipitated crystals were collected by filtration, washed, and dried to give the title compound (0.78 g, yield 56%) as colorless crystals.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07786165B2
Source datasetuspto-grants-2010_08
ORD IDord-3f4ec84d19f243be821d7cc20d38d471
Source noteuspto-grants-2010_08