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Methanesulfonic Acid → (S)-3-[4-(3-fluorobenzyloxy) benzylamino]pyrrolidin-2-one
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | Methanesulfonic Acid | HCID 6395 | — |
| 反応物 | 4-[(3-Fluorophenyl)methoxy]benzaldehyde | HCID 880119 | — |
| 反応物 | Sodium cyanoborohydride | HCID 5003444 | — |
| 反応物 | (3S)-3-aminopyrrolidin-2-one | HCID 12430456 | — |
| 溶媒 | Methanol | HCID 887 | — |
| 生成物 | (S)-3-[4-(3-fluorobenzyloxy) benzylamino]pyrrolidin-2-one | HCID 54532112 | — |
反応手順
To a 2M solution of (S)-3-aminopyrrolidin-2-one (1.47 g, 14.6 mmol), prepared as described in Example 5, in anhydrous methanol 2.0 g of 3 Å molecular sieves and 0.77 g NaBH3CN (12 mmol) were added; after 10 minutes, 3.4 g (14.8 mmol) of 4-(3-fluorobenzyloxy)benzaldehyde in 40 ml of anhydrous methanol were added. The reaction was carried out for 3 hours, then the mixture filtered, the solution was evaporated yielding a residue which was directly flash-chromatographed on silica gel (eluant: CHCl3:CH3OH:NH3 (30%) 97:3:0.3, v:v:v) to give a white solid (3.4 g; 74%). The free base thus obtained was treated with a stoichiometric amount of methanesulfonic acid to give the title compound m.p. 140.5-143.5° C.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US08063039B2 |
| 出典データセット | uspto-grants-2011_11 |
| ORD ID | ord-a96668a128a64b0b8680f1fb3af5ecf8 |
| 出典メモ | uspto-grants-2011_11 |