ChemicalBook CAS DataBase List 10-Hydroxycamptothecin

10-Hydroxycamptothecin synthesis

8synthesis methods

Product Name:10-Hydroxycamptothecin
CAS Number:19685-09-7
Molecular formula:C20H16N2O5
Molecular Weight:364.35

7689-03-4 Synthesis

7689-03-4
601 suppliers
$18.00/1g

19685-09-7
437 suppliers
$16.00/100mg

19685-11-1
4 suppliers
inquiry

Yield:-

Reaction Conditions:

Stage #1:camptothecin with hydrogen;acetic acid;platinum under 760.051 Torr; for 8.5 h;
Stage #2: with lead(IV) acetate in acetic acidHeating / reflux;

Steps:

I.A EXAMPLE I
A) 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 PtO₂in 80 ml of HOAc for 1.5 hr under 1 atmosphere hydrogen pressure) and acetic acid to 1 atm. of H₂for 8.5 h after which theoretical amount of H₂absorbed (slightly more than 0.4 l) and uptake of H₂gets 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 CHCl₃by 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).