HRID432014

反应详情

EQUATION

反应方程式

HRID 432014 的结构方程式

AUXILIARIES

试剂、催化剂与溶剂

1

PROCEDURE

实验过程

10-Hydroxycamptothecin was prepared by subjecting camptothecin (3.2 g 0.0092 mol), 0.8 g of Pt0 (prepared by pre-reduction of 8 g of amorphous PtO2 in 80 ml of HOAc for 1.5 hr under 1 atmosphere hydrogen pressure) and acetic acid to 1 atm. of H2 for 8.5 h after which theoretical amount of H2 absorbed (slightly more than 0.4 l) and uptake of H2 gets slowed down The reaction mixture was degassed under steam of Helium and filtered through celite and washed with HOAc (20 ml). The resulting solution of 1, 2, 6, 7 tetrahydroxy-camptothecin was treated immediately with Pb (OAc)4 (6.4 g 0.014 mol) in portions and reaction mixture, stirred vigorously under Helium for 30 min. Gumy residue was obtained on evaporation of solvent which was triturated with cold water (100 ml) to produce light brown solid. The solid was collected, washed with cold water and air dried overnight when a mixture of 10-HCPT (44%), 10-AcHOCPT (26%) and unreacted CPT (32%) on HPLC basis was obtained. This crude mixture was combined with 150 ml of 50% HOAc and heated under reflux conditions overnight The reaction mixture was cooled, concentrated to 20 ml and treated with cold water (100 ml) to produce precipitate, which is filtered, washed with more cold water and dried to afford 2.1 g of solid containing HCPT (70%) AcCPT (1.2%) and CPT (21.3%) on the basis HPLC. Mixture was triturating with 0.5% aq HCl to dissolve the water-soluble. When insoluble CPT was removed by filtration. Water-soluble was extracted with chloroform and crystallized from boiling solution of 20% of MeOH in CHCl3 by adding EtOAC dropwise until turbidity appeared to obtain pure yellow HCPT which gives orange colored spot on TLC (CHCl3, acetone, MeOH 7:2:1), C20H16N2O5 (m/s 364), mp 268-270° C. UV. λmax. 222, 266, 330 and 382 IR (KBr) 3480 (OH), 1740 (Lactone) and 1655 (pyridone) cm−1; 1H NMR 0.88 (t, 3, C-18), 1.85 (m, 2, C-19 CH3), 5.35 (s, 2, C-17), 6.40 (s, C-20 OH), 7.22 (s, 1H, C-14), 7.28 (m, C-11 and C-12), 7.26 (d, 1, C-9), 8.38 (1, s, C-7), 10.3 (s, br, C-10 OH).

WORKUP

后处理

  1. customabsorbed (slightly more than 0.4 l) and uptake of H2
  2. customwas degassed under steam of Helium
  3. filtrationfiltered through celite
  4. washwashed with HOAc (20 ml)
  5. customGumy residue was obtained on evaporation of solvent which
  6. customwas triturated with cold water (100 ml)
  7. customto produce light brown solid
  8. customThe solid was collected
  9. washwashed with cold water and air
  10. customdried overnight when
  11. additiona mixture of 10-HCPT (44%), 10-AcHOCPT (26%) and unreacted CPT (32%) on HPLC basis
  12. customwas obtained
  13. temperatureheated under reflux conditions overnight The reaction mixture
  14. temperaturewas cooled
  15. concentrationconcentrated to 20 ml
  16. additiontreated with cold water (100 ml)
  17. customto produce precipitate, which
  18. filtrationis filtered
  19. washwashed with more cold water
  20. customdried