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HRID 230017作成日:2026年10月25日

Hydrochloric Acid → 3-Bromo-4-{[(4-tert-butylcyclohexyl)(5-methoxy-1-methyl-1h-benzimidazol-2-yl)amino]methyl}benzoic acid

https://huagongshe.com/reaction/230017

反応式

関与物質

役割名称HCID仕込み量
反応物Hydrochloric AcidHCID 313—
反応物Lithium HydroxideHCID 3939—
反応物Ethyl AcetateHCID 8857—
反応物Methyl 3-bromo-4-{[(4-tert-butylcyclohexyl)(5-methoxy-1-methyl-1H-benz-imidazol-2-yl)amino]methyl}benzoateHCID 68837491—
溶媒WaterHCID 962—
溶媒1,4-DioxaneHCID 31275—
生成物3-Bromo-4-{[(4-tert-butylcyclohexyl)(5-methoxy-1-methyl-1h-benzimidazol-2-yl)amino]methyl}benzoic acidHCID 68838815—

反応条件

温度40 °C

反応手順

To the title compound of Example 224 Step D (0.07 mmol, 40 mg) in 2 mL of dioxane was added a solution of LiOH (1 mmol, 24 mg) in 1 mL of H2O. The reaction was allowed to stir at 40° C. for 1.5 h. The crude reaction mixture was poured into pH 7 buffer/EtOAc, which was acidified with 2 N HCl until two clear layers formed after agitation. The organic phase was collected and the aqueous phase was extracted twice with EtOAc. The combined organic phase was dried over Na2SO4, then concentrated under reduced pressure to afford the product as a slightly yellow-green foam. HPLC A: 2.32 min.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07563815B2
出典データセットuspto-grants-2009_07
ORD IDord-4776b4418b33418490a2decccacea137
出典メモuspto-grants-2009_07