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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1845896Generated: October 30, 2026

Nitrogen → HCID 89708471, compound

https://huagongshe.com/reaction/1845896

Reaction equation

Participants

RoleNameHCIDCharge
ReactantNitrogenHCID 947—
ReactantTriethylamineHCID 8471—
ReactantTrimethylsilylacetyleneHCID 66111—
Reactant5-Bromo-3-[(1S)-1-(2,6-dichloro-3-fluorophenyl)ethoxy]-2-pyridinamineHCID 84819346—
CatalystCopper iodideHCID 83717—
CatalystHCID 178418476HCID 178418476—
SolventTolueneHCID 1140—
ProductHCID 89708471HCID 8970847180.6%

Reaction Conditions

Temperature30 °C

Reaction Steps

The compound (S)-5-bromo-3-(1-(2,6-dichloro-3-fluorophenyl)ethoxy)-2-aminopyridine (12.58 g, 33.11 mmol) was dispersed in toluene (100 mL), and triethylamine (14.05 g, 139.06 mmol) and copper iodide (126 mg, 0.66 mmol) were added successively. Under the protection of N2 atmosphere, PdCl2(PPh3)2 (465 mg, 0.66 mmol) was added. The reaction mixture was heated to 30° C., stirred for 0.5 h. Ethynyltrimethylsilane (9.11 g, 92.71 mmol) was added dropwise, gradually warmed to 90° C., and stirred overnight. Through HPLC test, it was found that the raw materials were completely reacted. The reaction liquid was cooled down, washed with water, and the toluene layers were combined. The toluene layer was dried over anhydrous Na2SO4, concentrated; the residue was purified via silica gel column chromatography (petroleum ether:ethyl acetate=3:1) to yield the target product as yellow solid (10.6 g, yield: 80%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08952002B2
Source datasetuspto-grants-2015_02
ORD IDord-885d4328091247e39848fa7a4aae587a
Source noteuspto-grants-2015_02