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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1052625Generated: November 3, 2026

Pyridine → (S)-2-(1-((5-(1-(3-Methoxyphenyl)-1H-pyrazol-3-yl)-7-((2-(trimethylsilyl)ethoxy)methyl)-7H-pyrrolo[2,3-d]pyrimidin-4-yl)amino)ethyl)-5-methyl-3-phenylpyrrolo[2,1-f][1,2,4]triazin-4(3H)-one

https://huagongshe.com/reaction/1052625

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPyridineHCID 1049—
ReactantSodium CarbonateHCID 10340—
Reactant(3-Methoxyphenyl)boronic acidHCID 2734370—
ReactantHCID 178428095HCID 178428095—
CatalystCupric acetateHCID 8895—
SolventDimethylformamideHCID 6228—
Product(S)-2-(1-((5-(1-(3-Methoxyphenyl)-1H-pyrazol-3-yl)-7-((2-(trimethylsilyl)ethoxy)methyl)-7H-pyrrolo[2,3-d]pyrimidin-4-yl)amino)ethyl)-5-methyl-3-phenylpyrrolo[2,1-f][1,2,4]triazin-4(3H)-oneHCID 1317362409%

Reaction Conditions

Temperature75 °C

Reaction Steps

(S)-2-(1-((5-(1H-Pyrazol-3-yl)-7-((2-(trimethylsilyl)ethoxy)methyl)-7H-pyrrolo[2,3-d]pyrimidin-4-yl)amino)ethyl)-5-methyl-3-phenylpyrrolo[2,1-f][1,2,4]triazin-4(3H)-one (88 mg, 0.15 mmol) was dissolved in N,N-dimethylformamide (1.5 ml). (3-Methoxyphenyl)boronic acid (46 mg, 0.30 mmol), copper(II) acetate (4 mg, 0.02 mmol) and pyridine (28 μL, 0.34 mmol) were added and the mixture was stirred at 75° C. during 96 h. The reaction was poured into ice-water mixture, basified to pH 10 with sodium carbonate and extracted twice with ethyl acetate. The organics were combined and washed with water, brine, dried over sodium sulphate, filtered and evaporated under reduced pressure. The residue was purified using SP1® Purification System (0% to 50%, hexane-ethyl acetate) to give 9 mg (9% yield) of the title compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09388189B2
Source datasetuspto-grants-2016_07
ORD IDord-255ecc6891f24aa4808bc10f2d2c983d
Source noteuspto-grants-2016_07