Réaction #1951028

Équation de réaction

2,5,6-Trichloro-3-formyl-1-(β-D-ribofuranosyl)indole

asym-dimethylhydrazine

MeOH CHCl3

→

4.35

Rendement 78.0%

2,5,6-Trichloro-3-[N-(dimethylamino)iminomethylidene]-1-(β-D-ribofuranosyl)indole

Rendement 78.0%

Solvants

MeOH

DMF

Conditions de réaction

Traitement

1. 1
   Autreevaporated under vacuum
2. 2
   Autreto yield a yellow residue
3. 3
   workup.ADDITIONFractions containing product
4. 4
   Autreevaporated

Mode opératoire

2,5,6-Trichloro-3-formyl-1-(β-D-ribofuranosyl)indole (4.3, 100 mg, 0.26 mmol) was dissolved in MeOH (5 mL) to which was added asym-dimethylhydrazine (0.5 mL). The resulting solution was stirred at room temperature for 16 h, then evaporated under vacuum to yield a yellow residue. The residue was dissolved in DMF (0.5 mL) and subjected to column chromatography (40×350 mm) on silica gel with 10% MeOH/CHCl3. Fractions containing product were pooled and evaporated to yield 87 mg (78%) of 4.35 as a white powder: mp dec >170° C.; Rf0.4 (10% MeOH/CHCl3); 1H-NMR (500 MHz, DMSO-d6): δ 8.44 (s, 1H), 8.36 (s, 1H), 7.35 (s, 1H), 5.91 (d, 1H), 5.36-5.31 (m, 2H, D2O exch.), 5.21 (d, 1H, D2O exch.), 4.42 (q, 1H), 4.13 (s, 1H), 3.96 (d, 1H), 3.70 (b, 2H), 2.93 (s, 6H). 13C-NMR (125 MHz, DMSO-d6): δ 133.01, 125.64, 125.62, 125.37, 124.26, 124.04, 121.97, 114.85, 110.14, 88.58, 85.75, 71.18, 69.66, 61.14, 42.58. HRMS (ES) m/z calcd. for C16H18Cl3N3O4□Na 444.0261, found 444.0269. Anal calcd for C16H18Cl3N3O4: C, 45.46; H, 4.29; N, 9.94. Found: C, 45.79; H, 4.61; N, 10.06.

Source