Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1444641Generated: October 30, 2026

Methyl iodide → 4-(3-Adamantan-1-yl-ureido)butyric Acid Methyl Ester

https://huagongshe.com/reaction/1444641

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl iodideHCID 6328—
ReactantPotassium CarbonateHCID 11430—
Reactant4-(3-Adamantan-1-yl-ureido)butyric acidHCID 11425995—
SolventDimethylformamideHCID 6228—
Product4-(3-Adamantan-1-yl-ureido)butyric Acid Methyl EsterHCID 1143785595%

Reaction Steps

A mixture of 4-(3-adamantan-1-yl-ureido)butyric acid 822 (0.15 g, 0.54 mmol), K2CO3 (0.09 g, 0.64 mmol), and iodomethane (0.04 mL, 0.59 mmol) in DMF (20 mL) was stirred at room temperature for 20 h. Then the product was extracted with ether (20 mL), and the ether was washed with 1 N NaOH aqueous solution (20 mL) and brine (20 mL), dried over Na2SO4, and evaporated to afford 0.15 g (95%) of 883: 1H NMR (CDCl3) 1.66-1.68 (6H, m), 1.81 (2H, quint, J=6.9 Hz), 1.94-1.97 (6H, m), 2.05-2.07 (3H, m), 2.37 (2H, t, J=6.9 Hz), 3.16 (2H, q, J=6.9 Hz), 3.68 (3H, s), 4.09 (1H, s), 4.25 (1H, s); LC-MS (ESI) m/z calcd for C16H26N2O3 [M+H]+ 295.19, found [M+H]+ 295.24; mp 114 C. Anal. (C16H26N2O3) C, H, N.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07662910B2
Source datasetuspto-grants-2010_02
ORD IDord-f487971fe26b4ddbbaf9707aa1e824cc
Source noteuspto-grants-2010_02