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HRID 1173883作成日:2026年10月27日

Sodium Hydroxide → (4-{[bis(1H-imidazol-2-ylmethyl)-amino]-methyl}-phenyl)-[4-(1-propylbutyl)-piperazin-1-yl]-methanone

https://huagongshe.com/reaction/1173883

反応式

関与物質

役割名称HCID仕込み量
反応物Sodium HydroxideHCID 14798—
反応物4-HeptanoneHCID 31246—
反応物Sodium cyanoborohydrideHCID 5003444—
反応物(4-{[bis-(1H-imidazol-2-ylmethyl)-amino]-methyl}-phenyl)-piperazin-1-yl-methanoneHCID 21084462—
溶媒Acetic AcidHCID 176—
溶媒MethanolHCID 887—
溶媒TriethylamineHCID 8471—
生成物(4-{[bis(1H-imidazol-2-ylmethyl)-amino]-methyl}-phenyl)-[4-(1-propylbutyl)-piperazin-1-yl]-methanoneHCID 10344979—

反応手順

The compound (57.7 mg) obtained in Example 32-2 was dissolved in methanol (1.73 ml) and then added with 4-heptanone (manufactured by Tokyo Kasei Kogyo Co., Ltd.) (30.7 μl), sodium cyanoborohydride (13.8 mg), and triethylamine (76.5 μl). The solution was adjusted to pH 5 with acetic acid and stirred at room temperature for 7 days. The reaction solution was added with a 1 mol/l sodium hydroxide aqueous solution and then the whole was separated and extracted with chloroform. The organic layer was dried with anhydrous sodium sulfate. The solvent was distilled off and the residue was then purified through silica gel column chromatography (chloroform/methanol) and treated with hydrochloric acid, thereby obtaining hydrochloride (27.7 mg) of the subject compound as a pale-yellow solid.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07833991B2
出典データセットuspto-grants-2010_11
ORD IDord-c3bb52d9fe924e0abcada2fb1a6a212c
出典メモuspto-grants-2010_11