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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1478079Generated: October 30, 2026

Triethylamine → 3-(5-((5-chloro-2-((1,3-dimethyl-1H-pyrazol-4-yl)amino)pyrimidin-4-yl)amino)hexahydrocyclopenta[c]pyrrol-2(1H)-yl)-3-oxopropanenitrile

https://huagongshe.com/reaction/1478079

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—
Reactant5-chloro-N2-(1,3-dimethyl-1H-pyrazol-4-yl)-N4-(octahydrocyclopenta[c]pyrrol-5-yl) pyrimidine-2,4-diamineHCID 118390108—
SolventDimethylformamideHCID 6228—
SolventDichloromethaneHCID 6344—
Product3-(5-((5-chloro-2-((1,3-dimethyl-1H-pyrazol-4-yl)amino)pyrimidin-4-yl)amino)hexahydrocyclopenta[c]pyrrol-2(1H)-yl)-3-oxopropanenitrileHCID 11839004055.9%

Reaction Steps

To a solution of 5-chloro-N2-(1,3-dimethyl-1H-pyrazol-4-yl)-N4-(octahydrocyclopenta[c]pyrrol-5-yl)pyrimidine-2,4-diamine (186.6 mg, 0.54 mmol) and 2-cyanoacetic acid (64.8 mg, 0.76 mmol) in a mixture of DCM (20 mL) and DMF (5 mL) were added HATU (374.3 mg, 0.98 mmol) and Et3N (151.8 mg, 1.50 mmol). After addition, the reaction mixture was stirred at rt for 1 h, 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)=1/50) to give the title compound as a beige solid (124.5 mg, 55.9%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09403801B2
Source datasetuspto-grants-2016_08
ORD IDord-38d420be86a04342b041d41149e45083
Source noteuspto-grants-2016_08