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HRID 2110005作成日:2026年10月25日

Methanol → HCID 10238744、化合物

https://huagongshe.com/reaction/2110005

反応式

関与物質

役割名称HCID仕込み量
反応物MethanolHCID 887—
反応物5-Chloro-salicylaldehydeHCID 12481—
反応物Sodium triacetoxyborohydrideHCID 5049666—
反応物HCID 86610506HCID 86610506—
溶媒Dimethylsulfoxide acetic acidHCID 18355466—
生成物HCID 10238744HCID 10238744—

反応条件

温度50 °C

反応手順

After dissolving 2-[(piperidin-4-ylmethyl)-amino]-1H-benzimidazole-4-carboxylic acid (2-methoxy-ethyl)-amide (20 mg, 0.049 mmol) in dimethylsulfoxide-acetic acid (10:1, 0.50 ml), 2-hydroxy-5-chlorobenzaldehyde (23 mg, 0.15 mmol) and sodium triacetoxyborohydride (31 mg, 0.15 mg) were added and the mixture was stirred at 50° C. for 2 days. Methanol (1 ml) was added to the reaction mixture, and after stirring for 1 minute, the mixture was purified by SCX solid phase extraction (Bond Elute SCX500MG). The product was further purified by preparative HPLC to obtain 2-{[1-(5-chloro-2-hydroxy-benzyl)-piperidin-4-ylmethyl]-amino}-1H-benzimidazole-4-carboxylic acid (2-methoxy-ethyl)-amide. The compound was identified by LC-MS.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07517875B2
出典データセットuspto-grants-2009_04
ORD IDord-bcd1af0e36d94e9ab600e18a4845f604
出典メモuspto-grants-2009_04