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Pyridine → N-BOC-3(R)-methylsulfonyloxymethyl-piperidine
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | Pyridine | HCID 1049 | — |
| 反応物 | Methanesulfonyl chloride | HCID 31297 | — |
| 反応物 | tert-Butyl 3-(hydroxymethyl)piperidine-1-carboxylate | HCID 2763851 | — |
| 溶媒 | Dichloromethane | HCID 6344 | — |
| 生成物 | N-BOC-3(R)-methylsulfonyloxymethyl-piperidine | HCID 10108453 | — |
反応手順
To a stirred solution of N—BOC-3-piperidinemethanol (0.50 g, 0.002 mmole) in DCM (10 mL) was added dropwise pyridine (2.42 mL, 0.03 mmole) followed by the addition of methanesulfonyl chloride (0.774 mL, 0.01 mmole). The reaction mixture continued stirring at RT overnight. The reaction mixture was quenched with water. The aqueous layer was extracted with EtOAc (3×5 mL). Combined organic layers were dried over Na2SO4 and concentrated to yield a crude oil, 68, which was used in the next step without further purification. LRMS: 193 (M+-BOC group).
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US07816375B2 |
| 出典データセット | uspto-grants-2010_10 |
| ORD ID | ord-a94c232791c6417ca5b9f80a4945474c |
| 出典メモ | uspto-grants-2010_10 |