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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 416186Generated: October 30, 2026

Hydrochloric Acid → Fasiglifam

https://huagongshe.com/reaction/416186

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantMethanolHCID 887—
ReactantSodium HydroxideHCID 14798—
ReactantMethyl [(3S)-6-({2',6'-dimethyl-4'-[3-(methylsulfonyl)propoxy]biphenyl-3-yl}methoxy)-2,3-dihydro-1-benzofuran-3-yl]acetateHCID 57414917—
SolventWaterHCID 962—
SolventTetrahydrofuranHCID 8028—
ProductFasiglifamHCID 2485728688.4%

Reaction Conditions

Temperature50 °C

Reaction Steps

To a solution of methyl[(3S)-6-({2′,6′-dimethyl-4′-[3-(methylsulfonyl)propoxy]biphenyl-3-yl}methoxy)-2,3-dihydro-1-benzofuran-3-yl]acetate (0.438 g, 0.813 mmol) in a mixed solvent of methanol (2 mL) and tetrahydrofuran (4 mL) was added 2 M aqueous sodium hydroxide solution (1 mL), and the mixture was stirred at 50° C. for 2 hr. The reaction mixture was diluted with water, acidified with 1 M hydrochloric acid, and extracted with ethyl acetate. The extract was washed with saturated brine, dried over anhydrous magnesium sulfate, and concentrated under reduced pressure. The precipitated crystals were recrystallized from heptane-ethyl acetate to give the title compound (0.377 g, yield 88%) as colorless crystals.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08088821B2
Source datasetuspto-grants-2012_01
ORD IDord-2ad8f33f3b7847fd92ff400f9bfa74ae
Source noteuspto-grants-2012_01