関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | Amantadine | HCID 2130 | — |
| 反応物 | Potassium Carbonate | HCID 11430 | — |
| 反応物 | 3-[3-(3-Bromo-propoxy)phenyl]-thieno[2,3-d]isoxazole | HCID 21983559 | — |
| 溶媒 | Acetonitrile | HCID 6342 | — |
| 生成物 | Adamantan-1-yl-[3-(3-thieno[2,3-d]isoxazol-3-yl-phenoxy)-propyl]-amine | HCID 21983599 | 44% |
反応手順
Mix 3-[3-(3-bromo-propoxy)-phenyl]-thieno[2,3-d]isoxazole (0.250 g, 0.739 mmol), potassium carbonate (0.205 g, 1.48 mmol), 1-adamantanamine (0.560 g, 3.70 mmol) and acetonitrile (4.0 mL) and heat at 75° C., overnight. Cool the reaction mixture and filter through a Waters Sep-Pak (1 g) silica gel cartridge (ethyl acetate). Combine the appropriate fractions and concentrate to give a residue. Purify the residue by column (10 g silica) chromatography using a step gradient from 40% ethyl acetate in dichloromethane to 100% ethyl acetate to 20% methanol in ethyl acetate to give the title compound (132 mg, 44% yield). Purity by LC/MS (APCI)=98%, [M+H]+=409.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US07091199B1 |
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| 出典データセット | uspto-grants-2006_08 |
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| ORD ID | ord-7b4bedc2459741bd84e5d05b7da325ca |
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| 出典メモ | uspto-grants-2006_08 |
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