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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1253766Generated: November 3, 2026

Triethylamine → 5-(4-{4-[1-(2-Chloro-phenyl)-ethoxycarbonylamino]-3-methyl-isoxazol-5-yl}-phenyl)-pent-4-ynoic acid

https://huagongshe.com/reaction/1253766

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
Reactant4-Pentynoic acidHCID 22464—
Reactant[5-(4-Bromophenyl)-3-methylisoxazol-4-yl]carbamic acid 1-(2-chlorophenyl)ethyl esterHCID 67350786—
CatalystCopper iodideHCID 83717—
CatalystHCID 178418397HCID 178418397—
Solvent1,2-DimethoxyethaneHCID 8071—
Product5-(4-{4-[1-(2-Chloro-phenyl)-ethoxycarbonylamino]-3-methyl-isoxazol-5-yl}-phenyl)-pent-4-ynoic acidHCID 46213906—

Reaction Conditions

Temperature80 °C

Reaction Steps

[5-(4-Bromo-phenyl)-3-methyl-isoxazol-4-yl]-carbamic acid 1-(2-chloro-phenyl)-ethyl ester (0.200 g, 0.46 mmol), 4-pentynoic acid (0.054 g, 0.55 mmol), copper iodide (spatula tip), triethylamine (0.12 mL, 0.84 mmol), and tetrakis(triphenylphosphine)palladium(0) (0.053 g, 0.05 mmol) were combined in DME (5 mL), and the reaction was purged with N2 for 15 minutes and then stirred at 80° C. overnight. The mixture was partitioned between EtOAc and H2O, and the aqueous layer was separated and extracted with EtOAc. The combined organic layers were dried over MgSO4, filtered, and concentrated, and the residue was purified by preparative HPLC to give the title compound. Mass spec. data (M+H)=453.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08455499B2
Source datasetuspto-grants-2013_06
ORD IDord-ada0a0b0b2aa4defb6813a30a6aa2f2f
Source noteuspto-grants-2013_06