N-DESMETHYL TOPOTECAN synthesis
- Product Name:N-DESMETHYL TOPOTECAN
- CAS Number:190710-79-3
- Molecular formula:C22H21N3O5
- Molecular Weight:407.42
19685-09-7
421 suppliers
$16.00/100mg
593-51-1
525 suppliers
$21.00/100g
190710-79-3
22 suppliers
$100.00/100ug
Yield:190710-79-3 50 %
Reaction Conditions:
with formaldehyd;acetic acid in water at 80;Sealed tube;
Steps:
21.1 Step-1: Synthesis of (S)-4-Ethyl-4,9-dihydroxy-10-((methylamino)methyl)-l,12-dihydro-14H- pyrano[3',4':6,7]indolizino[l,2-b]quinoline-3,14(4H)-dione (Int-2)
To a stirred solution of (.S>4-cthyl-4,9-dihydroxy- 1 , 12-di hydro- 14//-pyrano[3',4':6,7|indoli/.ino[ 1 ,2- /?|qui no line-3, 14(4//)-dionc (Int-1, 2.0 g, 5.4 mmol, 1.0 eq.) and methyl amine hydrochloride (255 mg, 8.2 mmol, 1.5 eq.) in acetic acid (20 mL) was added 37% solution of formaldehyde (197 mg, 6.59 mmol, 1.2 eq.) at room temperature. The reaction mixture was heated to 80°C and stirred for 2 h in a sealed tube. Progress of the reaction was monitored by TLC. After completion of the reaction, solvents were evaporated under reduced pressure to get crude compound. The crude compound was basified with aq. ammonia until the pH reached to 9, filtered the solid and washed with water, dried under vacuum to afford Int-2 (1.7 g, 50%). 1H NMR (400 MHz, DMSO-ife) d 8.70 (s, 1H) 7.97 (d, J 9o.l2i9n Hz, 1H) 7.40 (d, J 9o.l2i9n Hz, 1H) 7.24 (s, 1H) 5.41 (s, 2H) 5.22 (s, 2H) 5.20 (br s, 1H) 4.37 (s, 2H) 2.46 (s, 3H) 1.82 - 1.93 (m, 3H) 0.88 (br t, / = 6.85 Hz, 3H). LCMS: 408.4 [M+H]+.
References:
WO2022/204184,2022,A1 Location in patent:Page/Page column 152-153
50-00-0
849 suppliers
$10.00/25g
19685-09-7
421 suppliers
$16.00/100mg
74-89-5
7 suppliers
$13.44/25ML
190710-79-3
22 suppliers
$100.00/100ug