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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 473632Generated: October 30, 2026

Propargyl alcohol → 3-(2-(4-(Pyridin-2-ylamino)phenoxy)pyridin-3-YL)prop-2-YN-1-OL

https://huagongshe.com/reaction/473632

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPropargyl alcoholHCID 7859—
ReactantTriethylamineHCID 8471—
ReactantN-(4-(3-Iodopyridin-2-yloxy)phenyl)pyridin-2-amineHCID 59373959—
CatalystCopper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI)HCID 24350—
CatalystHCID 178418476HCID 178418476—
SolventTetrahydrofuranHCID 8028—
Product3-(2-(4-(Pyridin-2-ylamino)phenoxy)pyridin-3-YL)prop-2-YN-1-OLHCID 59373956—

Reaction Steps

A mixture of N-(4-(3-iodopyridin-2-yloxy)phenyl)pyridin-2-amine (0.300 g, 0.771 mmol), copper(I) iodide (3.91 μL, 0.116 mmol), trans-dichlorobis(triphenyl-phosphine)palladium (II) (0.034 g, 0.048 mmol), triethylamine (0.800 mL, 5.74 mmol) and propargyl alcohol (0.150 mL, 2.54 mmol) in THF (5 mL) was stirred at rt under an atmosphere of argon for 3.5 h. The reaction was evaporated onto silica gel and purified by flash chromatography (Isco, (60 gram)) eluting with 2M NH3 in MeOH:CH2Cl2 (0:1→3:97). The material was stirred over MeOH, filtered and dried in vacuo to give a white crystalline solid. MS (ESI, pos. ion) m/z: 318.0. IC50 (uM)=0.2612.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08637500B2
Source datasetuspto-grants-2014_01
ORD IDord-d52139cd7bfe4774b7879c522f277c8e
Source noteuspto-grants-2014_01