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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 915253Generated: October 31, 2026

Diisopropylethylamine → N-(4-cyano-1-methyl-piperidin-4-yl)-2-(4-cyano-pyrimidin-2-ylamino)-3-cyclohexyl-propionamide

https://huagongshe.com/reaction/915253

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiisopropylethylamineHCID 81531—
Reactant2-Chloropyrimidine-4-carbonitrileHCID 246647—
Reactant2-amino-N-(4-cyano-1-methyl-piperidin-4-yl)-3-cyclohexyl-propionamideHCID 22063143—
SolventAcetonitrileHCID 6342—
ProductN-(4-cyano-1-methyl-piperidin-4-yl)-2-(4-cyano-pyrimidin-2-ylamino)-3-cyclohexyl-propionamideHCID 2206324852%

Reaction Steps

2-Chloro-4-pyrimidinecarbonitrile (0.3 mmol, Daves, G. D. Jr., O'Brien, D. E., Cheng, C. C. J. Het. Chem, 1964, 1, 130) and 2-amino-N-(4-cyano-1-methyl-piperidin-4-yl)-3-cyclohexyl-propionamide (0.7 mmol) were dissolved in acetonitrile (10 mL) containing N,N-diisopropylethylamine (0.6 mmol). The solution was heated to a gentle reflux for 17 h. The volatiles were evaporated and the residue was subjected to chromatography (silica gel, eluant=EtOAc then MeOH). The methanolic fraction was concentrated to a colorless solid which was rechromatographed (10% MeOH/EtOAc) to afford the title compound as a colorless solid (52%). The material was recrystallized from dichloromethane/petroleum ether.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07265132B2
Source datasetuspto-grants-2007_09
ORD IDord-9c942752024e4b0c9935f7083f59a9d5
Source noteuspto-grants-2007_09