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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
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | Hydrochloric Acid | HCID 313 | — |
| 反応物 | Lithium Hydroxide | HCID 3939 | — |
| 反応物 | Ethyl Acetate | HCID 8857 | — |
| 反応物 | Methyl 3-bromo-4-{[(4-tert-butylcyclohexyl)(5-methoxy-1-methyl-1H-benz-imidazol-2-yl)amino]methyl}benzoate | HCID 68837491 | — |
| 溶媒 | Water | HCID 962 | — |
| 溶媒 | 1,4-Dioxane | HCID 31275 | — |
| 生成物 | 3-Bromo-4-{[(4-tert-butylcyclohexyl)(5-methoxy-1-methyl-1h-benzimidazol-2-yl)amino]methyl}benzoic acid | HCID 68838815 | — |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US07563815B2 |
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| 出典データセット | uspto-grants-2009_07 |
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| ORD ID | ord-4776b4418b33418490a2decccacea137 |
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| 出典メモ | uspto-grants-2009_07 |
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