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HRID 1453579作成日:2026年10月25日

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

https://huagongshe.com/reaction/1453579

反応式

関与物質

役割名称HCID仕込み量
反応物BenzimidazoleHCID 5798—
反応物Dibenzyl etherHCID 7657—
反応物2,6-Dichloro-9-((2-(trimethylsilyl)ethoxy)methyl)-9H-purineHCID 58285232—
反応物HCID 178420378HCID 178420378—
溶媒1-ButanolHCID 263—
生成物2-chloro-6-[6-(phenylmethoxy)-1H-benzimidazol-1-yl]-9-[[2-(trimethylsilyl) ethoxy]methyl]-9H-purineHCID 8661410248.8%

反応条件

温度120 °C

反応手順

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.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07476670B2
出典データセットuspto-grants-2009_01
ORD IDord-f128de6f5f6748459fc36bcee54d9c29
出典メモuspto-grants-2009_01