반응 #6329

ord-7b19ffcc5e3d49d7a3afa6d58e690d43

반응 조건

상세 조건
See reaction.notes.procedure_details.

후처리

  1. 1
    온도to warm to 20°-25° during this time
  2. 2
    workup.ADDITIONAt the end of this time, a small amount of ice is added
  3. 3
    workup.ADDITIONis added slowly
  4. 4
    기타The solvent layers are separated
  5. 5
    추출the aqueous layer is extracted with additional methylene chloride (7×1 ml)
  6. 6
    건조The combined organic layers are dried over magnesium sulfate
  7. 7
    농축concentrated
  8. 8
    기타to provide an oil
  9. 9
    기타This oil is purified on a silica preparative plate (1000μ)

실험 절차

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.

출처

DOI: 10.6084/m9.figshare.5104873.v1특허: US05247090uspto-grants-1993_09