反応 #3773

ord-fbd154b2d6e642c8b3af3f1af09e77e0

反応方程式

O
water
O=C1[C@@H](N2C(=O)c3ccccc3C2=O)Cc2ccccc2C2CCC=CN12
(S)-7-[(1,3-dihydro-1,3-dioxo-2H-isoindol-2-yl)]-1,2,6,7,8,12b-hexahydro-6-oxopyrido[2,1-a][2]benzazepine
O=S(=O)(O)O
sulfuric acid
O=CO
formic acid
O=C(O)[C@@H]1CCCC2c3ccccc3CC(N3C(=O)c4ccccc4C3=O)C(=O)N21
title compound
O=C(O)[C@@H]1CCCC2c3ccccc3CC(N3C(=O)c4ccccc4C3=O)C(=O)N21
(S)-7-[(1,3-Dihydro-1,3-dioxo-2H-isoindol-2-yl)]-1,2,3,4,6,7,8,12b-octahydro-6-oxopyrido[2,1-a][2]benzazepine-4-carboxylic acid

反応条件

詳細条件
See reaction.notes.procedure_details.

後処理

  1. 1
    その他quickly seal the vessel
  2. 2
    抽出Extract the reaction mixture with ethyl acetate
  3. 3
    抽出Extract the organic layer with saturated aqueous potassium carbonate solution (5×10 mL)
  4. 4
    抽出Extract with chloroform (5×15 mL)
  5. 5
    乾燥Combine the organic layers, dry over MgSO4
  6. 6
    ろ過filter
  7. 7
    その他evaporate in vacuo
  8. 8
    その他to give a residue

実験手順

Combine (S)-7-[(1,3-dihydro-1,3-dioxo-2H-isoindol-2-yl)]-1,2,6,7,8,12b-hexahydro-6-oxopyrido[2,1-a][2]benzazepine (32 mg, 0.09 mmol) and sulfuric acid (1.0 mL, 95-98%) in a pressure vessel. Add 96% formic acid (200 μL) and quickly seal the vessel. After 18 hours, add water (10 mL). Extract the reaction mixture with ethyl acetate. Extract the organic layer with saturated aqueous potassium carbonate solution (5×10 mL). Combine the aqueous layers and carefully acidify with aqueous 12M hydrochloric acid solution. Extract with chloroform (5×15 mL). Combine the organic layers, dry over MgSO4, filter, and evaporate in vacuo to give a residue. Chromatograph the residue on silica gel eluting with 2/1 ethyl acetate/hexane containing 0.5% acetic acid to give the title compound. Rf =0.14 (silica gel, 2/1 ethyl acetate/hexane containing 0.5% acetic acid).

出典

DOI: 10.6084/m9.figshare.5104873.v1特許: US05734049uspto-grants-1998_03