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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2120664Generated: October 29, 2026

Pent-4-ynoic acid butyl ester → 5-[6-(4-Methoxy-benzylamino)-pyridin-2-yl]-pent-4-ynoic acid butyl ester

https://huagongshe.com/reaction/2120664

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPent-4-ynoic acid butyl esterHCID 23435506—
Reactant6-Bromo-(4-methoxybenzylamino)pyridineHCID 23435509—
CatalystCopper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI)HCID 24350—
SolventTriethylamineHCID 8471—
Product5-[6-(4-Methoxy-benzylamino)-pyridin-2-yl]-pent-4-ynoic acid butyl esterHCID 6966603379.6%

Reaction Steps

To a mixture of 6-2 (8.64 g, 29.48 mmol) and 6-4 (5.0 g, 32.4 mmol) in Et3N (50 mL) at 0° was added CuI (0.14 g, 0.74). The solution was purged with argon and [(C6H5)3P]2PdCl2 (0.52 g, 0.74 mmol) was added. After 1 h the cooling bath was removed and the solution was stirred for an additional 12 h. The solution was diluted with diethyl ether (250 mL) and washed with water (4×100 ml) followed by brine (100 mL). The etheral layer was dried (Na2SO4), concentrated, and chromatographed (silica gel, 30% ethyl acetate/hexanes) to give 8.6 g of 6-5.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06693101B2
Source datasetuspto-grants-2004_02
ORD IDord-79c0443949284053a7658ea67212914b
Source noteuspto-grants-2004_02