関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | Sodium hydride | HCID 24758 | — |
| 反応物 | 3-Methylxanthine | HCID 70639 | — |
| 反応物 | 3,5-Bis(benzyloxy)-alpha-chlorotoluene | HCID 74339 | — |
| 触媒 | Tetrabutylammonium Iodide | HCID 67553 | — |
| 溶媒 | Water | HCID 962 | — |
| 溶媒 | Dimethylformamide | HCID 6228 | — |
| 生成物 | HCID 71521071 | HCID 71521071 | 78% |
反応手順
A solution of 3-methyl xanthine (200 mg, 1.2 mmol) in N,N-dimethylformamide (5 ml) was treated with 3,4-bis-benzyloxy-benzyl chloride (Lot #PRO-04-36B, 1.02 g, 3 mmol) and NaH (96 mg, 4 mmol) and 0.5 equivalent tetrabutyl ammonium iodide and was heated to 60° C. for 12 hrs. The reaction mixture was poured in water and extracted with ethyl acetate (3×30 ml). The combined organic extract was washed with water, brine solution (30 ml) each and dried over anhydrous magnesium sulfate. The solvent was removed under reduced pressure and the product was purified by flash column chromatography over silica gel using 40% ethyl acetate/hexane to yield the desired product, 600 mg, 78% yield. This product was dissolved in ethyl acetate (25 ml) and methanol (10 ml) and acetic acid (1 ml) and hydrogenated in presence of 10% Pd—C at 55 PSI for 2 hr. Catalyst was filtered off and the solvent was removed under reduced pressure. The residue was purified on a silica gel column eluting with 50% ethyl acetate in hexane to 100% ethyl acetate. The desired product was isolated as an off white solid, Yield=400 mg PD 151.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US09169255B2 |
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| 出典データセット | uspto-grants-2015_10 |
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| ORD ID | ord-8c8b592e3b714cb9a35323b83574cd2d |
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| 出典メモ | uspto-grants-2015_10 |
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