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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2091090Generated: November 1, 2026

Sodium Hydroxide → HCID 66777847, compound

https://huagongshe.com/reaction/2091090

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium HydroxideHCID 14798—
ReactantHCID 66777646HCID 66777646—
SolventEthanolHCID 702—
SolventTetrahydrofuranHCID 8028—
SolventEthanol hexaneHCID 21879635—
ProductHCID 66777847HCID 6677784798%

Reaction Steps

Ethyl 3-{[(4-{[cyclopentyl(5-fluoro-3-methyl-1-benzofuran-2-yl)methyl]amino}phenyl)carbonyl](methyl)amino}propanoate (4.18 g) obtained in Example A67(5) was dissolved in hexane-ethanol (1:1, volume ratio), subjected to HPLC using CHIRALPAK AD (50 mm ID×500 mL, manufactured by Daicel Chemical Industries, Ltd.), and eluted with hexane-ethanol (1:1, volume ratio) as a mobile phase at 30° C. and at a flow rate 60 mL/min. The resulting fraction containing an optically active form having a longer retention time was concentrated to give an amorphous form (2.04 g, 99.9% ee). The obtained amorphous form (2.04 g) was dissolved in ethanol (9 mL) and tetrahydrofuran (9 mL), 1N aqueous sodium hydroxide solution (8.5 mL) was added, and the mixture was stirred at room temperature for 30 min. The solvent was evaporated under reduced pressure, water (15 mL) was added, and the mixture was neutralized with 1N hydrochloric acid (8.5 mL) under ice-cooling, and stirred for 1 hr. The resulting precipitate was collected by filtration, and dried to give the title compound (1.88 g, 98%, 99.9% ee) as a colorless amorphous form.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08436043B2
Source datasetuspto-grants-2013_05
ORD IDord-87800c352dde485e983ef12e06a2003e
Source noteuspto-grants-2013_05