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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

反応式

関与物質

役割名称HCID仕込み量
反応物Benzyltrimethylammonium hydroxideHCID 66854—
反応物Ethyl trans-2-hexenoateHCID 5364778—
反応物1-1,2-Benzisoxazol-3-ylmethyl-1,3-dihydro-benzimidazol-2-oneHCID 59497602—
溶媒DimethylformamideHCID 6228—
溶媒Ammonium ChlorideHCID 25517—
生成物3-(3-1,2-Benzisoxazol-3-ylmethyl-2-oxo-2,3-dihydro-benzimidazol-1-yl)-hexanoic acid ethyl esterHCID 5949731846%

反応条件

温度60 °C

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

DOI10.6084/m9.figshare.5104873.v1
特許番号US09150556B2
出典データセットuspto-grants-2015_10
ORD IDord-1f6ce19c6ca245a2bce6eeb1e70ff29f
出典メモuspto-grants-2015_10