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HRID 883684作成日:2026年10月27日

Ammonia → 1-{3-[benzyl(methyl)amino]propyl}-2-[(3,5-dimethoxy phenyl)amino]-N,N-diisobutyl-1H-benzimidazole-5-carboxamide Hydrochloride

https://huagongshe.com/reaction/883684

反応式

関与物質

役割名称HCID仕込み量
反応物AmmoniaHCID 222—
反応物Hydrochloric AcidHCID 313—
反応物TetrahydrofuranHCID 8028—
反応物4-Isothiocyanato-1,2-dimethoxybenzeneHCID 141856—
反応物3-amino-4-({3-[benzyl(methyl)amino]propyl}amino)-N,N-diisobutylbenzamideHCID 69028792—
溶媒Diethyl EtherHCID 3283—
生成物1-{3-[benzyl(methyl)amino]propyl}-2-[(3,5-dimethoxy phenyl)amino]-N,N-diisobutyl-1H-benzimidazole-5-carboxamide HydrochlorideHCID 69029031—

反応手順

3,4 dimethoxyphenylisothiocyanate (35 mg, 1.2 eq) and N-methylcyclohexylcarbodiimide-N-methyl-polystyrene resin (acquired from Novabiochem; charge 1.69 mmol/g, 355 mg, 4 eq) are added successively to a solution of 3-amino-4-({3-[benzyl(methyl)amino]propyl}amino)-N,N-diisobutylbenzamide (65 mg, 1 eq) in tetrahydrofuran (2 ml). The mixture is heated under reflux for 18 hours then cooled down to ambient temperature and aminomethyl polystyrene resin (acquired from Novabiochem, 2 eq) is added. After stirring for 4 hours at ambient temperature, the mixture is filtered on frit and the filtrate is concentrated under reduced pressure at 40° C. The residue obtained is dissolved in ethyl ether and a 1N solution of HCl in ethyl ether is added dropwise in order to produce the expected compound in the form of the hydrochloride salt (81 mg, 92% yield).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08236965B2
出典データセットuspto-grants-2012_08
ORD IDord-62ff4ce5971943e39aa2364d058d22ae
出典メモuspto-grants-2012_08