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Dichloromethane piperidine → (3R)-3-Butyl-2,5-piperazinedione
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | Dichloromethane piperidine | HCID 67144590 | — |
| 反応物 | Methyl N-{[(9H-fluoren-9-ylmethyl)oxy]carbonyl}-D-norleucylglycinate | HCID 67401200 | — |
| 溶媒 | Dichloromethane | HCID 6344 | — |
| 生成物 | (3R)-3-Butyl-2,5-piperazinedione | HCID 67400830 | — |
反応手順
A solution of methyl N-{[(9H-fluoren-9-ylmethyl)oxy]carbonyl}-D-norleucylglycinate from step (a) above (2 g, 4.7 mmol) in a 7:3 mixture of dichloromethane/piperidine (30 mL) was stirred at room temperature for 0.75 h. The reaction mixture was diluted with dichloromethane (200 mL) and solid which precipitated was filtered, washed with cold DCM (2×50 mL) and dried in vacuo to give the title compound as a white solid. MS (ESI, positive ion) m/z: 171 (M+1).
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US08026241B2 |
| 出典データセット | uspto-grants-2011_09 |
| ORD ID | ord-5de44db36eea43b2b9e94ed22a6f09a2 |
| 出典メモ | uspto-grants-2011_09 |