تفاعل #90866

ord-79f55600219c4c2a8d67961975ee03d9

المذيبات

ظروف التفاعل

الظروف التفصيلية
See reaction.notes.procedure_details.

المعالجة

  1. 1
    أخرىwas removed under vacuum
  2. 2
    workup.DISSOLUTIONThe mixture was dissolved in CHCl3
  3. 3
    غسيلwashed with H2O
  4. 4
    أخرىthe organic phase was separated
  5. 5
    تجفيفdried over Na2SO4
  6. 6
    أخرىevaporated
  7. 7
    أخرىPurification
  8. 8
    غسيلeluting with CH2Cl2—CH2Cl2

الإجراء التجريبي

To a stirred solution of Mono-Propargyl Curcumin 5 (63 mg, 0.16 mmol) and 2-(2-(2-azidoethoxy)ethoxy)ethanol (46 mg, 0.26 mmol) in tBuOH (1.1 mL) and CHCl3 (0.3 mL) was added a prepared solution of Cu(OAc)2 (8 mg, 0.03 mmol) and sodium ascorbate (13 mg, 0.07 mmol) in H2O (1.3 mL). After vigorous stirring overnight the solvent was removed under vacuum. The mixture was dissolved in CHCl3, washed with H2O and the organic phase was separated, dried over Na2SO4 and evaporated. Purification was performed by column chromatography, eluting with CH2Cl2—CH2Cl2: MeOH 98:2. Yield 26%. NMR 1H (CDCl3), δ (ppm): 3.55-3.60 (m, 8H); 3.72-3.72 (t, 3H); 3.87-3.94 (m, 8H); 4.54-4.55 (t, 2H); 5.80 (s, 1H); 6.07 (s, 1H); 6.46-6.50 (dd, 2H); 6.92-6.94 (d, 1H); 7.05-7.12 (m, 5H); 7.56-7.60 (q, 2H); 7.92 (s, 1H).). MS (ESI) calcd. for C30H35N3O9: 581.61. found: 582.3 [M+H]+, 604.3 [M++Na], 620.3 [M++K].

المصدر

DOI: 10.6084/m9.figshare.5104873.v1براءة الاختراع: US09447023B2uspto-grants-2016_09