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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1422478Generated: October 30, 2026

Iodine → 6-Chloro-2-iodo-9-isopropyl-9H-purine

https://huagongshe.com/reaction/1422478

Reaction equation

Participants

RoleNameHCIDCharge
ReactantIodineHCID 807—
ReactantDiiodomethaneHCID 6346—
ReactantIsoamyl NitriteHCID 8053—
ReactantSodium BicarbonateHCID 516892—
Reactant6-Chloro-9-isopropyl-9h-purin-2-amineHCID 21933771—
CatalystCopper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI)HCID 24350—
SolventTetrahydrofuranHCID 8028—
Product6-Chloro-2-iodo-9-isopropyl-9H-purineHCID 6538904—

Reaction Steps

6-chloro-9-isopropyl-9H-purin-2-amine (2.68 g, 12.7 mmol) was dissolved in THF (64 mL) at rt. Iodine (1.61 g, 6.25 mmol), CH2I2 (10.6 mL) and CuI (1.27 g, 6.66 mmol) were added. The mixture was stirred for 5 min at room temperature. Isopentyl nitrite (5.33 mL) was added. The reaction mixture was refluxed for 45 min, and was then cooled to room temperature. Saturated aqueous sodium bicarbonate solution was added, and the mixture was extracted with EtOAc three times. The combined organic phase was washed with brine, dried with MgSO4 and concentrated. The residue was purified by column chromatography on silica gel, eluting with 0 to 30% ethyl acetate in hexane to afford the title compound as a solid. 1H NMR (400 MHz, CDCl3) δ 8.09 (s, 1H), 4.95-4.88 (m, 1H), 1.65 (d, 6H). MS m/z 323.0 (M+1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08927281B2
Source datasetuspto-grants-2015_01
ORD IDord-1531000c6b9246cabcdd91027c75b2ed
Source noteuspto-grants-2015_01