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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 451236Generated: October 30, 2026

Ethanol → Bilastine

https://huagongshe.com/reaction/451236

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthanolHCID 702—
ReactantWaterHCID 962—
ReactantSodium HydroxideHCID 14798—
ReactantBilastine EsterHCID 45257628—
SolventAcetic AcidHCID 176—
Solvent1-ButanolHCID 263—
SolventEthyl AcetateHCID 8857—
ProductBilastineHCID 18546090%

Reaction Steps

In a reaction vessel, 2-[4-(2-{4-[1-(2-ethoxy-ethyl)-1H-benzoimidazol-2-yl]-piperidin-1-yl}-ethyl)-phenyl]-2-methyl-propionic acid methylester (2.3 g) prepared in the Example 14, sodium hydroxide (0.6 g) and ethylalcohol (13 mL) were introduced, and the mixture was reacted at 50-55□ for 3 hours. Distilled water (20 mL) was added thereto, and acetic acid was added to control the pH to 7. Ethylacetate (50 mL) was added thereto, and the mixture was stirred to separate a layer. The separated organic layer was condensed under reduced pressure. And, butanol (9 mL) was added thereto, and dissolved by heating. And then, it was cooled to precipitate crystals, and the crystals were filtered under reduced pressure to obtain 2-[4-(2-{4-[1-(2-ethoxy-ethyl)-1H-benzoimidazol-2-yl]-piperidin-1-yl}-ethyl)-phenyl]-2-methyl-propionic acid (2.0 g, yield 90%, HPLC purity 99% or more).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08487106B2
Source datasetuspto-grants-2013_07
ORD IDord-df4022744de849e6ae6130c32a81c108
Source noteuspto-grants-2013_07