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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1444640Generated: October 26, 2026

Gamma-Aminobutyric Acid → 4-(3-Adamantan-1-yl-ureido)butyric acid

https://huagongshe.com/reaction/1444640

Reaction equation

Participants

RoleNameHCIDCharge
ReactantGamma-Aminobutyric AcidHCID 119—
ReactantHydrochloric AcidHCID 313—
ReactantDimethylformamideHCID 6228—
Reactant1-IsocyanatoadamantaneHCID 2059995—
Product4-(3-Adamantan-1-yl-ureido)butyric acidHCID 11425995100%
Product4-(3-Adamantan-1-yl-ureido)butyric Acid Methyl EsterHCID 11437855—

Reaction Steps

The title compound was prepared by a procedure described in J. Med. Chem. 2004, 47, 2110. To a suspension of 4-aminobutyric acid (2.79 g, 27.1 mmol) in DMF (40 mL) was added 1-adamantyl isocyanate (1.20 g, 6.77 mmol) at room temperature. The reaction mixture was stirred for 24 h. Then 1 N HCl aqueous solution (40 mL) was added into the reaction, and the mixture was stirred for 30 min. The solid crystalline product was filtered and washed with water (20 mL) and ethyl acetate (20 mL). The resulting solid was dried in a vacuum oven to give 1.90 g (100%) of 4-(3-adamantan-1-yl-ureido)butyric acid 822 as a white solid: 1H NMR (CD3OD): 1.66-1.75 (8H, m), 1.94-1.97 (6H, m), 2.05-2.07 (3H, m), 2.30 (2H, t, J=6.9 Hz), 3.08 (2H, q, J=6.9 Hz), 3.32 (2H, s); LC-MS (ESI) m/z calcd for C15H24N2O3 [M+H]+ 281.18, found [M+H]+ 281.25; mp 165 C. Anal. (C15H24N2O3) C, H, N.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07662910B2
Source datasetuspto-grants-2010_02
ORD IDord-90a8a418ddec493f83a3dc911b9a5a16
Source noteuspto-grants-2010_02