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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2217747Generated: October 25, 2026

1-Pentyne → rac-5-{2-Hydroxy-3-[1-(2-fluoro-5-trifluoromethylphenyl)-cyclopropyl]-2-(pentin-1-yl)-propionylamino}phthalide

https://huagongshe.com/reaction/2217747

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-PentyneHCID 12309—
ReactantAmmonium ChlorideHCID 25517—
Reactant5-{3-[1-(2-Fluoro-5-trifluoromethylphenyl)-cyclopropyl]-2-oxo-propionylamino}-phthalideHCID 68871207—
ReactantButyllithiumHCID 178418339—
SolventTetrahydrofuranHCID 8028—
Productrac-5-{2-Hydroxy-3-[1-(2-fluoro-5-trifluoromethylphenyl)-cyclopropyl]-2-(pentin-1-yl)-propionylamino}phthalideHCID 58900311—

Reaction Conditions

Temperature-78 °C

Reaction Steps

A solution that consists of 1-pentyne (0.94 ml) in THF (9 ml) was mixed at −78° C. with nBuLi (0.6 ml, 1.6 M in hexane). It was allowed to stir for 30 minutes at −78° C., and then a solution of 5-{3-[1-(2-fluoro-5-trifluoromethylphenyl)-cyclopropyl]-2-oxopropionylamino}phthalide (200 mg) in 3 ml of tetrahydrofuran was added. Then, it was allowed to come to 23° C. over about 3 hours, and it was stirred for 10 more hours at this temperature. Then, the reaction mixture was poured into ice-cold, saturated ammonium chloride solution. It was extracted with ethyl acetate. The combined organic phases were washed with saturated sodium chloride solution and dried on sodium sulfate. The crude product was chromatographed on silica gel. 130 mg of product was obtained.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07408060B2
Source datasetuspto-grants-2008_08
ORD IDord-e2804a25e87146d99b97bf44ed998b56
Source noteuspto-grants-2008_08