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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 444675Generated: October 26, 2026

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

https://huagongshe.com/reaction/444675

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 numberUS08476043B2
Source datasetuspto-grants-2013_07
ORD IDord-da54b4a98396482e887b5790f7362497
Source noteuspto-grants-2013_07