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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 333411Generated: October 30, 2026

Diisopropylethylamine → HCID 178490377, compound

https://huagongshe.com/reaction/333411

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiisopropylethylamineHCID 81531—
ReactantO-(Benzotriazol-1-yl)-N,N,N',N'-tetramethyluronium tetrafluoroborateHCID 2733207—
Reactant4-Phenylpiperidine-4-carbonitrile hydrochlorideHCID 3084973—
ReactantHCID 178490381HCID 178490381—
SolventDimethylformamideHCID 6228—
SolventDichloromethaneHCID 6344—
ProductHCID 178490377HCID 17849037717%

Reaction Steps

To 300 mg (0.90 mmol) of 2-{3-[2-(1H-imidazol-4-yl)ethyl]ureido}-3-(4-methoxy-phenyl)propanoic acid dissolved in 3.5 mL of dichloromethane and 1.5 mL of dimethylformamide are added 0.46 mL (2.7 mmol) of diisopropylethylamine, 318 mg (0.99 mmol) of TBTU and 220 mg (0.99 mmol) of 4-cyano-4-phenylpiperidine hydrochloride. After 16 hours, the solution is washed with saturated sodium hydrogen carbonate solution and the organic products are extracted with dichloromethane. The organic phase is dried over magnesium sulfate, filtered and concentrated. The crude product obtained is purified by filtration on a pad of silica (eluent: 7/3 dichloromethane/methanol). 75 mg of 1-[2-(4-cyano-4-phenylpiperidin-1-yl)-1-(4-methoxybenzyl)-2-oxoethyl]-3-[2-(1H-imidazol-4-yl)ethyl]urea in the form of a white powder are obtained in a yield of 17%.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08877968B2
Source datasetuspto-grants-2014_11
ORD IDord-828d5a7d6b8443ea96684b9e139dcc0b
Source noteuspto-grants-2014_11