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HRID 1747357作成日:2026年10月27日
Benzyltrimethylammonium hydroxide → 3-(3-1,2-Benzisoxazol-3-ylmethyl-2-oxo-2,3-dihydro-benzimidazol-1-yl)-hexanoic acid ethyl ester
https://huagongshe.com/reaction/1747357
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | Benzyltrimethylammonium hydroxide | HCID 66854 | — |
| 反応物 | Ethyl trans-2-hexenoate | HCID 5364778 | — |
| 反応物 | 1-1,2-Benzisoxazol-3-ylmethyl-1,3-dihydro-benzimidazol-2-one | HCID 59497602 | — |
| 溶媒 | Dimethylformamide | HCID 6228 | — |
| 溶媒 | Ammonium Chloride | HCID 25517 | — |
| 生成物 | 3-(3-1,2-Benzisoxazol-3-ylmethyl-2-oxo-2,3-dihydro-benzimidazol-1-yl)-hexanoic acid ethyl ester | HCID 59497318 | 46% |
反応手順
To a stirred solution of 1-1,2-benzisoxazol-3-ylmethyl-1,3-dihydro-benzimidazol-2-one (100 mg, 0.38 mmol) in DMF (5 ml) was added ethyl trans-2-hexenoate (80 mg, 0.57 mmol) followed by benzyltrimethylammonium hydroxide (Triton B, 40 wt % in MeOH, 17.0 ul). The resulting mixture was warmed to 60° C. for 12 h and cooled to ambient temperature. The reaction was diluted with NH4Cl (sat.) and the product was extracted into ethyl acetate (2×). The combined organics were dried (MgSO4), filtered and concentrated to give the crude product which was purified via column chromatography (silica gel, 5% EtOAc/dichloromethane). The product-containing fractions were combined and concentrated to give 70 mg (46%) of the desired product.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US09150556B2 |
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| 出典データセット | uspto-grants-2015_10 |
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| ORD ID | ord-1f6ce19c6ca245a2bce6eeb1e70ff29f |
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| 出典メモ | uspto-grants-2015_10 |
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