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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1478051Generated: October 31, 2026

Triethylamine → HCID 118390092, compound

https://huagongshe.com/reaction/1478051

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantCyanoacetic acidHCID 9740—
ReactantMethanaminium, N-((dimethylamino)(3H-1,2,3-triazolo(4,5-b)pyridin-3-yloxy)methylene)-N-methyl-, hexafluorophosphate(1-) (1:1)HCID 9886157—
ReactantHCID 118390086HCID 118390086—
SolventDimethylformamideHCID 6228—
SolventDichloromethaneHCID 6344—
ProductHCID 118390092HCID 11839009287.1%

Reaction Steps

To a solution of 2-(4-((5-chloro-4-((octahydrocyclopenta[c]pyrrol-5-yl)amino)pyrimidin-2-yl)amino)-1H-pyrazol-1-yl)ethanol (0.29 g, 0.80 mmol) and 2-cyanoacetic acid (87.2 mg, 1.03 mmol) in a mixture of DCM (20 mL) and DMF (5 mL) were added HATU (462.4 mg, 1.22 mmol) and Et3N (0.17 g, 1.68 mmol). After addition, the reaction mixture was stirred at rt for 1 h, then quenched with H2O (30 mL) and extracted with DCM (100 mL×3). The combined organic phases were washed with brine (100 mL), dried over anhydrous Na2SO4, filtered and concentrated in vacuo. The residue was purified by silica gel column chromatography (MeOH/DCM (v/v)=1/20) to give the title compound as a beige solid (300.1 mg, 87%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09403801B2
Source datasetuspto-grants-2016_08
ORD IDord-9c2f0d047a444040a7eabdb50cb1b253
Source noteuspto-grants-2016_08