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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 4230Generated: October 26, 2026

Methanol → N'-[2-(Diethylamino)ethyl]-N-(1-methylethyl)-N-[5-(phenylsulfonyl)pentyl]urea hydrate

https://huagongshe.com/reaction/4230

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanolHCID 887—
ReactantN,N-DiethylethylenediamineHCID 60993—
Reactant1,1'-CarbonyldiimidazoleHCID 68263—
ReactantN-(1-methylethyl)-5-(phenylsulfonyl)-1-pentanamineHCID 13655070—
SolventChloroformHCID 6212—
SolventTetrahydrofuranHCID 8028—
ProductN'-[2-(Diethylamino)ethyl]-N-(1-methylethyl)-N-[5-(phenylsulfonyl)pentyl]urea hydrateHCID 2015283766.6%

Reaction Steps

A solution of 1,1'-carbonyldiimidazole (4.54 g, 0.028 mole) and N,N-diethylethylenediamine (2.90 g, 0.025 mole) in tetrahydrofuran was stirred for 1 hr at room temperature. A solution of N-(1-methylethyl)-5-(phenylsulfonyl)-1-pentanamine (6.74 g, 0.025 mole) in tetrahydrofuran (dried over 4 A molecular sieves) was added and the resulting solution was heated over night at gentle reflux. The reaction mixture was stripped to dryness and the residue dissolved in chloroform. The chloroform layer was extracted with water, dried (anhydrous sodium sulfate), filtered and the solvent removed to give a brown oil. The brown oil was subjected to flash column chromatography on Silica Gel using methanol for elution. Fractions of similar purity were combined, solvent removed, and the oil dried in vacuo at 60° C. overnight. This produced 7.00 g (66.6% yield) of brown oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04724235
Source datasetuspto-grants-1988_02
ORD IDord-3bf903c0996240489547e5913b65a55e
Source noteuspto-grants-1988_02