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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 551761Generated: November 1, 2026

Boron trifluoride etherate → 5-[4-(3-Methoxy-pyridin-2-yl)-oxazol-2-yl]-pentanoic acid methyl ester

https://huagongshe.com/reaction/551761

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBoron trifluoride etherateHCID 8000—
ReactantMethyl 6-amino-6-oxohexanoateHCID 14266897—
Reactant2-Bromo-1-(3-methoxy-pyridin-2-yl)-ethanoneHCID 59027825—
SolventTetrahydrofuranHCID 8028—
Product5-[4-(3-Methoxy-pyridin-2-yl)-oxazol-2-yl]-pentanoic acid methyl esterHCID 5902782833.4%

Reaction Conditions

Temperature80 °C

Reaction Steps

Add boron trifluoride etherate (0.30 mL, 1.00 mmol) to a sealed tube containing 2-bromo-1-(3-methoxy-pyridin-2-yl)-ethanone (231 mg, 1.00 mmol), 5-carbamoyl-pentanoic acid methyl ester (222 mg, 1.39 mmol), and THF (anhydrous, 3 mL). Flush with N2, seal, heat at 80° C. overnight. Partition between saturated aqueous NaHCO3 solution and 20% i-PrOH/CHCl3, separate layers. Extract from aqueous layer with 20% i-PrOH/CHCl3 (×3), dry combined organic layers with MgSO4 and concentrate. Adsorb on SiO2 and purify by flash chromatography on silica gel eluting with 1-3% methanol/CHCl3 to afford the title compound (97 mg, 33%). MS (IS) 291 (M+1)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07947841B2
Source datasetuspto-grants-2011_05
ORD IDord-f6186240b7fe43fabefd6f0007fda820
Source noteuspto-grants-2011_05