関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | Methyl 4-aminobenzoate | HCID 12082 | — |
| 反応物 | Diisopropylethylamine | HCID 81531 | — |
| 反応物 | PMID26882240-Compound-8 | HCID 625381 | — |
| 反応物 | Ethylcarbodiimide hydrochloride | HCID 21883477 | — |
| 反応物 | HCID 178527226 | HCID 178527226 | — |
| 溶媒 | Dimethylformamide | HCID 6228 | — |
| 生成物 | Methyl 4-({[4-(1-adamantyl)phenoxy]acetyl}amino)benzoate | HCID 3470321 | 51.7% |
反応手順
To a mixture of [4-(1-adamantyl)phenoxy]acetic acid (143.2 mg, 0.5 mmol), 4-aminobenzoic acid methyl ester (113.4 mg, 0.5 mmol), N-3-dimethylaminopropyl)-N′-ethyl carbodiimide HCl (EDC) (143.8 mg, 0.75 mmol) and 1-hydroxybenzothiazole (HOBt) (101.4 mg, 0.75 mmol) in DMF (6 mL) was added N,N-diisopropylethylamine, redistilled (DIPEA) (97.0 mg, 0.13 mL, 0.75 mmol). The mixture was stirred overnight, and then partitioned between ethyl acetate and 10% HCl. The organic phase was washed with brine, dried (MgSO4 anh), and concentrated. The residue was purified by silica gel flash column chromatography (n-Hexane:Ethyl acetate:MeOH=6:3:1) to give 4-[2-(4-Adamantan-1-yl-phenoxy)-acetylamino]-benzoic acid methyl ester as a white solid (108.3 mg, 51.7% yield).
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US08394799B2 |
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| 出典データセット | uspto-grants-2013_03 |
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| ORD ID | ord-5bb3175da738406fa5654c450b5e71e7 |
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| 出典メモ | uspto-grants-2013_03 |
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