Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2264882Generated: October 30, 2026

Acetonitrile → HCID 178439997, compound

https://huagongshe.com/reaction/2264882

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetonitrileHCID 6342—
ReactantBenzyl iodideHCID 12098—
Reactant2-Chloro-9-[2-deoxy-3,5-di-o-(p-toluoyl)-beta-d-erythro-pentofuranosyl]-6-(2-propylimidazol-1-yl)purineHCID 16088088—
ProductHCID 178439997HCID 178439997—

Reaction Steps

2-Chloro-9-[2-deoxy-3,5-di-O-(p-toluoyl)-β-D-erythro-pentofuranosyl]-6-(2-propylimidazol-1-yl)purine (0.615 g, 1 mmol) was treated with a solution of BnI in CH3CN (0.3 M, 40 mL, 12 mmol) by method 3 to give 3-benzyl-1-{2-chloro-9-[2-deoxy-3,5-di-O-(p-toluoyl)-β-D-erythro-pentofuranosyl]purin-6-yl}-2-propylimidazolium iodide (0.83 g, crude): 1H NMR (500 MHz, CDCl3) δ 8.94 (s, 1H), 8.49 (s, 1H), 8.00 (d, J=8.5 Hz, 2H), 7.88 (d, J=8.0 Hz, 2H), 7.81 (s, 1H), 7.46-7.50 (m, 5H), 7.32 (d, J=8.0 Hz, 2H), 7.25 (d, J=8.0 Hz, 2H), 6.67 (t, J=7.3 Hz, 1H), 5.75-5.85 (m, 3H), 4.71-4.82 (m, 3H), 3.67-3.74 (m, 2H), 2.99-3.02 (m, 2H), 2.47 (s, 3H), 2.42 (s, 3H), 1.75-1.81 (m, 2H), 1.17 (t, J=7.5 Hz, 3H); HRMS m/z 705.2606 (M+[C39H38ClN6O5=705.2592]).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07855285B2
Source datasetuspto-grants-2010_12
ORD IDord-a640059402774ab39eff1d9d7ef81a77
Source noteuspto-grants-2010_12