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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1827844Generated: November 2, 2026

Diisopropylethylamine → HCID 178465356, compound

https://huagongshe.com/reaction/1827844

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiisopropylethylamineHCID 81531—
Reactant2-amino-N-(-4-cyano-1-methyl-piperidin-4-yl)-3-cyclohexylpropionamide bis hydrochloride saltHCID 22566339—
ReactantMethyl N-(ethylcarbamoyl)benzenecarboximidateHCID 69416768—
SolventMethanolHCID 887—
ProductHCID 178465356HCID 17846535643%

Reaction Steps

A solution of 1-ethyl-3-(methoxy-phenyl-methylene)-urea (350 mg, 1.70 mmol), 2-amino-N-(4-cyano-1-methyl-piperidin-4-yl)-3-cyclohexyl-propionamide bis hydrochloride salt (512 mg, 1.40 mmol) and N,N-diisopropylethylamine (352 mg, 2.73 mmol) in dry methanol (5.0 mL) was stirred at room temperature for 60 h. The reaction mixture was concentrated and the resulting residue was chromatographed over 50 g of flash silica gel using dichloromethane to 5% methanol in dichloromethane as the eluant. This provided the desired product as a light yellow solid (280 mg, 43%) which was further purified by HPLC using a 20×250 mm C18 reverse phase column with the method being 20% acetonitrile in water to 90% acetonitrile in water. MS, m/z 467=M+1.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07056915B2
Source datasetuspto-grants-2006_06
ORD IDord-f1475bf665c24030ac1021d15ea750bb
Source noteuspto-grants-2006_06