Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1894859Generated: October 27, 2026

Water → N-(2,6-diisopropylphenyl)-2-[(1-phenylamino-cyclohexylmethyl)amino]acetamide

https://huagongshe.com/reaction/1894859

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantDimethylformamideHCID 6228—
Reactant2-Chloro-N-(2,6-diisopropylphenyl)acetamideHCID 2363774—
Reactant(1-Amino-methylcyclohexyl)phenylamineHCID 68630087—
ProductN-(2,6-diisopropylphenyl)-2-[(1-phenylamino-cyclohexylmethyl)amino]acetamideHCID 2522715671%

Reaction Conditions

Temperature100 °C

Reaction Steps

340 mg (1.34 mmol) of 2-chloro-N-(2,6-diisopropylphenyl)acetamide (obtained in Example 3/c) are added to 270 mg (1.32 mmol) of (1-amino-methylcyclohexyl)phenylamine (obtained in Example 2/b) in 10 ml of dimethylformamide. The reaction medium is stirred at 100° C. under microwave irradiation for 30 min. It is then poured into water and extracted with ethyl acetate. The organic phases are collected and washed with water and then dried over sodium sulfate. The solvents are evaporated. The residue is chromatographed on silica gel (heptane/ethyl acetate 80/20, v/v). 396 mg of N-(2,6-diisopropylphenyl)-2-[(1-phenylaminocyclohexylmethyl)-amino]acetamide are obtained in the form of a white solid. M.p. 104-6° C., yield=71%.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08513307B2
Source datasetuspto-grants-2013_08
ORD IDord-a98c3384440c460fb1311e685c759ecf
Source noteuspto-grants-2013_08