関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | L-Methionine | HCID 6137 | — |
| 反応物 | Ammonium Chloride | HCID 25517 | — |
| 反応物 | Lithium Hexamethyldisilazide | HCID 2733832 | — |
| 反応物 | Benzyl 4-cyanopiperidine-1-carboxylate | HCID 22028286 | — |
| 溶媒 | Tetrahydrofuran | HCID 8028 | — |
| 生成物 | Benzyl 4-cyano-4-methylpiperidine-1-carboxylate | HCID 66980706 | 80.3% |
反応手順
LiHMDS (47.6 mL, 47.6 mmol) was added dropwise via syringe to the mixture of benzyl 4-cyanopiperidine-1-carboxylate (8.00 g, 31.8 mmol, [Oakwood]) in THF (50 mL) at about −78° C. and stirred for about 1 h. Met (6.76 g, 47.6 mmol) was added dropwise via syringe at about −78° C. and the mixture was stirred overnight at rt. The solution was cooled to 0° C. and saturated aqueous NH4Cl (200 mL) was added. The mixture was extracted with DCM (3×300 mL). The combined organic extracts were dried over anhydrous Na2SO4, filtered and concentrated in vacuo. The sample was deposited onto silica gel and purified by column chromatography eluting with 10:1 pet ether/EtOAc to give benzyl 4-cyano-4-methylpiperidine-1-carboxylate (6.6 g, 74%): LC/MS (Table 2, Method i) Rt=2.03 min; MS m/z: 259 (M+H)+.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US08551981B2 |
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| 出典データセット | uspto-grants-2013_10 |
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| ORD ID | ord-636345933a4e4599a0d0118cb39ab536 |
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| 出典メモ | uspto-grants-2013_10 |
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