Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2229378Generated: October 30, 2026

Diisopropylethylamine → HCID 178473534, compound

https://huagongshe.com/reaction/2229378

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiisopropylethylamineHCID 81531—
Reactant2-Chloro-1-methylpyridinium iodideHCID 167069—
ReactantEthyl (morpholin-4-ylcarbonothioyl)carbamateHCID 2824559—
Reactant2-amino-N-(-4-cyano-1-methyl-piperidin-4-yl)-3-cyclohexylpropionamide bis hydrochloride saltHCID 22566339—
SolventCitric AcidHCID 311—
SolventDichloromethaneHCID 6344—
ProductHCID 178473534HCID 17847353426%

Reaction Steps

2-Chloro-N-methylpyridinium iodide (680 mg, 2.66 mmol), was added to a solution of (Morpholine-4-carbothioyl)-carbamic acid ethyl ester (450 mg, 2.06 mmol), 2-amino-N-(4-cyano-1-methyl-piperidin-4-yl)-3-cyclohexyl-propionamide bis hydrochloride salt (745 mg, 2.04 mmol), and N,N-diisopropylethylamine (1.10 mL, 6.3 mmol) in dichloromethane (8.0 mL). The reaction was stirred at room temperature for 2.5 h then taken up in 10% citric acid solution and washed with EtOAc. The aqueous phase was then basified with saturated sodium carbonate and extracted with EtOAc. The organic extract was dried (MgSO4) and concentrated to provide the desired product as a white solid (250 mg, 26%). This material 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 477=M+1.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06420364B1
Source datasetuspto-grants-2002_07
ORD IDord-865b5fe9a2364a33ab6c54a42a668bdd
Source noteuspto-grants-2002_07