関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | Ammonium Hydroxide | HCID 14923 | — |
| 反応物 | Methyl 5-bromothiophene-2-carboxylate | HCID 605713 | — |
| 反応物 | N-Boc-pyrrolidine | HCID 643455 | — |
| 反応物 | Sparteine | HCID 644020 | — |
| 反応物 | Tri-t-butylphosphine fluoroborate | HCID 44558591 | — |
| 反応物 | CID 53628100 | HCID 178418400 | — |
| 触媒 | palladium(II) acetate | HCID 167845 | — |
| 触媒 | Zincchloride | HCID 3007855 | — |
| 溶媒 | Diethyl Ether | HCID 3283 | — |
| 溶媒 | Cyclohexane | HCID 8078 | — |
| 溶媒 | tert-Butyl methyl ether | HCID 15413 | — |
| 生成物 | (R)-tert-butyl 2-(5-methoxycarbonylthiophen-2-yl)pyrrolidine-1-carboxylate | HCID 66758892 | — |
反応手順
To a solution of N-Boc-pyrrolidine (3 mL) and (−)-sparteine (3.9 mL) in tert-butyl methyl ether (36 mL) at −78° C. was added 1.4M sec-butyl lithium in cyclohexane (12.21 mL). The solution was stirred for 3 hours and 1M zinc chloride in ether (10.2 mL) was added. The mixture was stirred for 30 minutes and warmed to ambient temperature for 30 minutes. Methyl 5-bromothiophene-2-carboxylate (3.15 g), tri-tert-butylphosphine tetrafluoroborate (249 mg) and palladium(II) acetate (153 mg) were added, and the mixture was stirred at ambient temperature overnight, treated with concentrated ammonium hydroxide (1 mL) and stirred for 30 minutes, and filtered through diatomaceous earth (Celite®). The filtrate was washed with 0.5M hydrochloric acid solution and water and concentrated. The concentrate was flash chromatographed on silica gel with ethyl acetate/hexane.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US08067613B2 |
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| 出典データセット | uspto-grants-2011_11 |
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| ORD ID | ord-6c310ccc24894e758f571d8f23d9781f |
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| 出典メモ | uspto-grants-2011_11 |
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