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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1453579Generated: October 25, 2026

Benzimidazole → 2-chloro-6-[6-(phenylmethoxy)-1H-benzimidazol-1-yl]-9-[[2-(trimethylsilyl) ethoxy]methyl]-9H-purine

https://huagongshe.com/reaction/1453579

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzimidazoleHCID 5798—
ReactantDibenzyl etherHCID 7657—
Reactant2,6-Dichloro-9-((2-(trimethylsilyl)ethoxy)methyl)-9H-purineHCID 58285232—
ReactantHCID 178420378HCID 178420378—
Solvent1-ButanolHCID 263—
Product2-chloro-6-[6-(phenylmethoxy)-1H-benzimidazol-1-yl]-9-[[2-(trimethylsilyl) ethoxy]methyl]-9H-purineHCID 8661410248.8%

Reaction Conditions

Temperature120 °C

Reaction Steps

860 mg of product obtained in stage 1 above are mixed with 605 mg of 5-(phenylmethoxy)-1H-benzimidazole (benzyl ether in the 5-position of benzimidazole) and 15 ml of butanol. The mixture is heated at 120° C. for 24 hours. Partial drying, washing with H2O and then drying under vacuum at 50° C. are carried out. 667 mg of 2-chloro-6-[6-(phenylmethoxy)-1H-benzimidazol-1-yl]-9-[[2-(trimethylsilyl)ethoxy]methyl]-9H-purine are obtained, in the form of beige-colored crystals.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07476670B2
Source datasetuspto-grants-2009_01
ORD IDord-f128de6f5f6748459fc36bcee54d9c29
Source noteuspto-grants-2009_01