تفاعل #3773

ord-fbd154b2d6e642c8b3af3f1af09e77e0

معادلة التفاعل

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

المذيبات

ظروف التفاعل

الظروف التفصيلية
See reaction.notes.procedure_details.

المعالجة

  1. 1
    أخرىquickly seal the vessel
  2. 2
    استخلاصExtract the reaction mixture with ethyl acetate
  3. 3
    استخلاصExtract the organic layer with saturated aqueous potassium carbonate solution (5×10 mL)
  4. 4
    استخلاصExtract with chloroform (5×15 mL)
  5. 5
    تجفيفCombine the organic layers, dry over MgSO4
  6. 6
    ترشيحfilter
  7. 7
    أخرىevaporate in vacuo
  8. 8
    أخرىto give a residue

الإجراء التجريبي

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).

المصدر

DOI: 10.6084/m9.figshare.5104873.v1براءة الاختراع: US05734049uspto-grants-1998_03