반응 #531811

ord-c1e82def16f14b04a2919076228764f8

반응 방정식

CC(C)(C)OC(=O)NCC(=O)NCC(=O)NCC(=O)O
t-Boc-GlyGlyGly
NCC(=O)NCC(=O)NCC(=O)O
12
NCC(=O)NCC(=O)NCC(=O)O
GlyGlyGly

반응 조건

상세 조건
See reaction.notes.procedure_details.

후처리

  1. 1
    기타Solvent was removed under vacuum
  2. 2
    workup.DISSOLUTIONthe residue was re-dissolved in methylene chloride
  3. 3
    workup.ADDITIONThe solution was poured into ether
  4. 4
    기타to give instant precipitate (yellow)
  5. 5
    여과The precipitate was filtered
  6. 6
    세척washed with cold ether

실험 절차

t-Boc-GlyGlyGly (1.359 g, 4.7 mmol) was dissolved in 350 mL of anhydrous methylene chloride at room temperature and to this solution were added DIPC (0.75 mL, 4.7 mmol), DMAP (382 mg, 3.13 mmol) and camptothecin (0.55 g, 1.57 mmol) at 0° C. The reaction mixture was allowed to warm to room temperature and left for 16 h. The solution was washed with 0.1 N HCl, dried and evaporated under reduced pressure to yield a white solid, which was recrystallized from methanol to give camptothecin-20-ester of t-Boc-GlyGlyGly: 1H NMR (DMSO-d6) δ 8.40 (s), 8.25 (d), 7.91 (d), 7.78 (m), 7.65 (t), 7.26 (s), 7.05 (br, s), 5.65 (d), 5.40 (d), 5.25 (s), 5.10 (br, s), 3.75-4.42 (m), 2.15-2.35 (m), 1.45 (s), 0.95 (t) Camptothecin-20-ester of t-Boc-GlyGlyGly (1.5 g, 1.06 mmol) was dissolved in a mixture of methylene chloride (10 mL) and TFA (10 mL) and stirred at room temperature for 1 h. Solvent was removed under vacuum and the residue was re-dissolved in methylene chloride. The solution was poured into ether to give instant precipitate (yellow). The precipitate was filtered and washed with cold ether to give 1.31 g of 12. 1H NMR (DMSO-d6) δ 8.79 (s), 7.75-8.61 (m), 7.10 (s), 5.55 (s), 3.90-4.37 (m), 3.86 (s), 3.54 (s), 2.11-2.23 (m), 0.95 (t). ESI/MS (m/z) expected 519; Found 520 (M+H).

출처

DOI: 10.6084/m9.figshare.5104873.v1특허: US08475781B2uspto-grants-2013_07