反応 #6329
ord-7b19ffcc5e3d49d7a3afa6d58e690d43
反応方程式
反応物
試薬
反応条件
後処理
- 1温度to warm to 20°-25° during this time
- 2workup.ADDITIONAt the end of this time, a small amount of ice is added
- 3workup.ADDITIONis added slowly
- 4その他The solvent layers are separated
- 5抽出the aqueous layer is extracted with additional methylene chloride (7×1 ml)
- 6乾燥The combined organic layers are dried over magnesium sulfate
- 7濃縮concentrated
- 8その他to provide an oil
- 9その他This oil is purified on a silica preparative plate (1000μ)
実験手順
Acetic anhydride (91 μl) is added to a mixture of (±) (1S,9aS/1R,9aR) N-[(9,9a-dihydro-3-oxo-1H,3H-oxazolo[3,4-a]indol-1-yl)methyl]acetamide (X diastereomer B, EXAMPLE 11, 74 mg) in methane sulfonic acid (1 ml) at 0° over 1 minute. The mixture is stirred for 20.5 hours and allowed to warm to 20°-25° during this time. At the end of this time, a small amount of ice is added and the mixture is diluted with methylene chloride. To this mixture of sodium bicarbonate (2.4 g) is added slowly. The solvent layers are separated and the aqueous layer is extracted with additional methylene chloride (7×1 ml). The combined organic layers are dried over magnesium sulfate and concentrated to provide an oil. This oil is purified on a silica preparative plate (1000μ) by developing it in methanol/methylene chloride (5/95, 3×) which provides the title compound, NMR (CDCl3, 300 MHz) 7.88, 7.84, 7.43, 6.40, 4.62, 4.57, 3.75, 3.36, 3.13, 2.58 and 2.08 δ; CMR (CDCl3, 75.47 MHz) 23.15, 26.62, 34.24, 41.02, 61.84, 83.26, 114.37, 125.53, 129.86, 132.98, 134.2, 144.1, 154.7, 170.6 and 196.5 δ; IR (CHCl3) 3660, 3440, 2980, 2920, 1760, 1670, 1600, 1480, 1420, 1350, 1260, 1120, 1050, 980 and 700 cm-1 ; MS (m/e) 288, 244, 229, 216, 201, 185, 170, 160, 144, 130, 118, 85, 73 and 43, exact mass calcd for C15H16 --N2O4 (288.1110), found 288.1105.