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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1023446Generated: October 25, 2026

Triethylamine → [4-(2-Methoxy-phenylethynyl)-pyridin-2-yl]-carbamic acid tert-butyl ester

https://huagongshe.com/reaction/1023446

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
Reactant1-Ethynyl-2-methoxybenzeneHCID 582912—
Reactant(4-Iodo-Pyridin-2-Yl)-Carbamic Acid Tert-Butyl EsterHCID 11484026—
CatalystCopper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI)HCID 24350—
CatalystHCID 178418476HCID 178418476—
SolventDimethylformamideHCID 6228—
SolventEthyl AcetateHCID 8857—
Product[4-(2-Methoxy-phenylethynyl)-pyridin-2-yl]-carbamic acid tert-butyl esterHCID 69085398—

Reaction Steps

A mixture of (4-iodo-pyridin-2-yl)-carbamic acid tert-butyl ester (250.0 mg, 0.781 mmol), 1-ethynyl-2-methoxy-benzene (93.8 mg, 0.710 mmol), CuI (13 mg, 0.071 mmol), Pd(PPh3)2Cl2 (25 mg, 0.036 mmol), and Et3N (9 mL) in dry DMF (3 mL) is stirred at room temperature for 19 hours. The reaction is diluted with ethyl acetate (20 mL) and quenched with saturated aqueous NH4Cl (10 mL). The organic layer is washed with an additional portion of saturated aqueous NH4Cl (10 mL), dried over MgSO4, filtered and concentrated. The residue is purified on SiO2 (0-30% ethyl acetate in heptanes, gradient) to give the product.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08722709B2
Source datasetuspto-grants-2014_05
ORD IDord-31ed2e9c0411466eadbbaec9b5b52ee6
Source noteuspto-grants-2014_05