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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1436635Generated: October 27, 2026

Oxazole → N-Methyl-5-oxazol-2-yl-N-propyl-isophthalamic acid methyl ester

https://huagongshe.com/reaction/1436635

Reaction equation

Participants

RoleNameHCIDCharge
ReactantOxazoleHCID 9255—
ReactantMethyl 3-iodo-5-{[methyl(propyl)amino]carbonyl}benzoateHCID 21086185—
ReactantButyllithiumHCID 178418339—
CatalystZincchlorideHCID 3007855—
CatalystBis(dibenzylideneacetone)palladiumHCID 9811564—
SolventDiethyl EtherHCID 3283—
SolventTetrahydrofuranHCID 8028—
ProductN-Methyl-5-oxazol-2-yl-N-propyl-isophthalamic acid methyl esterHCID 6881610782%

Reaction Conditions

Temperature-78 °C

Reaction Steps

Add n-butyllithium (1.6 M in hexanes, 1.25 mL, 2.01 mmol) dropwise to a solution of oxazole (126 mg, 1.83 mmol) in THF (12.6 mL) at −78° C. Stir for 30 min at −78° C. and add a solution of zinc chloride (747 mg, 5.49 mmol) in diethyl ether (5.5 mL) and stir at 0° C. for 1 h. Add a solution of 5-iodo-N-methyl-N-propyl-isophthalamic acid methyl ester (330 mg, 0.91 mmol) in THF (5.1 mL) followed by tetrakis(triphenylphosphine)palladium (0) (105 mg, 0.091 mmol) and heat to reflux for 30 min. Add ethyl acetate (40 mL), wash with water (2×20 mL), dry (magnesium sulfate), concentrate and purify (silica gel chromatography, eluting with 50:50 ethyl acetate:hexane) to give the title compound (225 mg, 82%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07618978B2
Source datasetuspto-grants-2009_11
ORD IDord-0efb2fd9500a41b2bb87eb1f1f93f735
Source noteuspto-grants-2009_11