Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1064612Generated: October 27, 2026

Ethyl bromoacetate → (2-Amino-6-iodopurin-9-yl)-acetic acid ethyl ester

https://huagongshe.com/reaction/1064612

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl bromoacetateHCID 7748—
ReactantPotassium CarbonateHCID 11430—
Reactant2-Amino-6-iodopurineHCID 6101575—
SolventDimethylformamideHCID 6228—
Product(2-Amino-6-iodopurin-9-yl)-acetic acid ethyl esterHCID 8584953195%

Reaction Steps

To a solution of 2-amino-6-iodo-purine (78.3 g, 0.3 mol) in DMF (1960 mL) was added ethyl bromoacetate (55.1 g, 0.33 mol) and potassium carbonate (82.9 g, 0.6 mol). The resulting reaction mixture was stirred for 12 h at room temperature. The reaction mixture was concentrated to small volume (about 150 mL) in vacuo and the residue was dissolved in water. The solid was filtered off, washed with water and ethyl ether, and dried in vacuo to give the titled compound (98.4 g, 95%). 1H-NMR (500 MHz; DMSO-d6) δ 8.06 (s, 1H), 6.90 (br.s, 2H), 4.94 (s, 2H), 4.17 (q, 2H), 1.22 (t, 3H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06969766B2
Source datasetuspto-grants-2005_11
ORD IDord-a267b75389da41458027017f3e95593b
Source noteuspto-grants-2005_11