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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1026362Generated: November 1, 2026

Triethylamine → tert-butyl [(1S)-2-(4-{[5-(cyclopropylmethoxy)pyridin-2-yl]ethynyl}-3,5-difluorophenoxy)-1-methylethyl]carbamate

https://huagongshe.com/reaction/1026362

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
Reactant2-Bromo-5-(cyclopropylmethoxy)pyridineHCID 57821796—
Reactanttert-butyl [(1S)-2-(4-ethynyl-3,5-difluorophenoxy)-1-methylethyl]carbamateHCID 86666330—
CatalystCopper iodideHCID 83717—
CatalystTriphenylphosphine palladium dichlorideHCID 13169693—
SolventTolueneHCID 1140—
Producttert-butyl [(1S)-2-(4-{[5-(cyclopropylmethoxy)pyridin-2-yl]ethynyl}-3,5-difluorophenoxy)-1-methylethyl]carbamateHCID 8666632935.9%

Reaction Conditions

Temperature100 °C

Reaction Steps

A mixture of tert-butyl [(1S)-2-(4-ethynyl-3,5-difluorophenoxy)-1-methylethyl]carbamate (2.5 g), 2-bromo-5-(cyclopropylmethoxy)pyridine (1.8 g), copper iodide (I) (0.15 g), dichloropalladium-triphenylphosphine (1:2) (0.56 g) and triethylamine (2.2 mL) in toluene (20 mL) was stirred at 100° C. overnight under argon atmosphere. After cooling to room temperature, the mixture was filtered through a pad of Celite. The filtrate was concentrated under reduced pressure. The residue was purified by silica gel column chromatography (hexane/ethyl acetate) to afford the title compound (1.3 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08729102B2
Source datasetuspto-grants-2014_05
ORD IDord-3418d85dd2534fa4b0cb79079f66eb44
Source noteuspto-grants-2014_05