関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | 1-Hydroxybenzotriazole hydrate | HCID 2796029 | — |
| 反応物 | 3-chloro-4-(2-methylpropyl)Benzoic acid | HCID 59316720 | — |
| 反応物 | HCID 178513316 | HCID 178513316 | — |
| 溶媒 | Dimethylformamide | HCID 6228 | — |
| 生成物 | (4-(5-(3-Chloro-4-isobutylphenyl)-1,2,4-oxadiazol-3-yl)phenyl)methanol | HCID 70869326 | — |
反応手順
N,N-Dicyclohexylcarbodiimide (1.07 g, 0.0052 mol) is added to a solution of 3-chloro-4-isobutylbenzoic acid (0.74 g, 0.0035 mol), N-hydroxy-4-hydroxymethylbenzamidine (0.867 g, 0.0052 mol) and N-hydroxybenzotriazole monohydrate (0.798 g, 0.0052 mol) in N,N-dimethylformamide (15 mL). The reaction mixture is heated at 120-125° C. for 2 hrs. It is then cooled to 0-5° C., filtered and washed with dichloromethane (2×20 mL). The filtrate is evaporated under reduced pressure and the residue is treated with demineralized water (20 mL). It is extracted with ethyl acetate (2×30 mL) and the combined extract is dried over sodium sulfate. Removal of solvent under reduced pressure gives a crude residue which is purified by column chromatography (silica gel 230-400, ethyl acetate:toluene, 15:85) to give {4-[5-(3-chloro-4-isobutylphenyl)-[1,2,4]-oxadiazol-3-yl]-phenyl}methanol.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US09266867B2 |
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| 出典データセット | uspto-grants-2016_02 |
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| ORD ID | ord-009c44ae601f4be8b37956c68656d75a |
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| 出典メモ | uspto-grants-2016_02 |
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