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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 610776Generated: October 25, 2026

Potassium Carbonate → N-cycloheptyl-5-[benzyl{2-(3-(aminocarbonylamino)phenoxy)ethyl}amino]pentanamide

https://huagongshe.com/reaction/610776

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
Reactantm-HydroxyphenylureaHCID 12796—
ReactantN-cycloheptyl-5-[benzyl(2-chloroethyl)amino]pentanamideHCID 22125964—
SolventDimethylformamideHCID 6228—
ProductN-cycloheptyl-5-[benzyl{2-(3-(aminocarbonylamino)phenoxy)ethyl}amino]pentanamideHCID 22125977—

Reaction Conditions

Temperature20 °C

Reaction Steps

Potassium carbonate (0.92 g, 6.6 mmole) is added to a solution of 3-hydroxyphenylurea (1 g, 6.6 mmole) in dimethylformamide (20 ml) and said mixture is stirred for 10 minutes at 20° C. A solution of N-cycloheptyl-5-[benzyl-(2-chloroethyl)amino]pentanamide (2.21 g, 6 mmole) in dimethylformamide (20 ml) is then added dropwise, the mixture being kept under agitation for 4 hours at 80° C. The solvent is evaporated under reduced pressure, then the residue is taken up in dichloromethane (50 ml) and washed with water. The organic phase is collected and dried then, after evaporation of the solvent, the desired compound is obtained in the form of an oil. It is purified by flash chromatography over silica gel in a mixture of dichloromethane/methanol (95/5) to give 1.75 g (60%) of pure compound. NMR-1H (CDCl3),;1.30-1.90 (m, 16H), 2.12 (t, 2H, J=6 Hz), 2.53 (t, 2H, J=6 Hz), 2.80 (t, 2H, J=6 Hz), 3.63 (s, 2H), 3.95 (m, 1H), 4.07 (t, 2H, J=6 Hz), 4.93 (s, 1H), 5.55 (m, 1H), 6.68 (m, 2H), 7.19 -7.30 (m, 9H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05998666
Source datasetuspto-grants-1999_12
ORD IDord-e3dedee516d44c37a0e50c81c92f8e2e
Source noteuspto-grants-1999_12