Réaction #62743

Équation de réaction

2,4-diamino-5-(7,8-dimethoxy-2H-1-benzopyran-5-ylmethyl)pyrimidine

m-chloroperbenzoic acid

→

2,4-Diamino-5-(7,8-dimethoxy-2H-1-benzopyran-5-ylmethyl)pyrimidine-1-oxide

Solvants

DMF

DMF

Conditions de réaction

Traitement

1. 1
   Autrethe solvent was evaporated
2. 2
   Autrethe residue chromatographed on silica gel
3. 3
   Lavageeluted with 10-15% methanol-methylene chloride
4. 4
   AutreRecovered
5. 5
   Lavageeluted first (0.40 g)
6. 6
   AutreRecrystallization from absolute ethanol
7. 7
   Autregave white crystals, mp 233°-234° dec.

Mode opératoire

To a solution of 2,4-diamino-5-(7,8-dimethoxy-2H-1-benzopyran-5-ylmethyl)pyrimidine (0.993 g, 3.16 mmol) in DMF (80 mL) was added a solution of m-chloroperbenzoic acid (0.641 g, 3.16 mmol as 85%) in DMF (10 mL) dropwise over 30 min. After 18 hr, the solvent was evaporated and the residue chromatographed on silica gel eluted with 10-15% methanol-methylene chloride. Recovered starting material eluted first (0.40 g) followed by title compound as a white powder (0.47 g). Recrystallization from absolute ethanol gave white crystals, mp 233°-234° dec.; assignment of N-1 oxide based on 13C-NMR: C-4 shifts from 154.40 to 161.28 ppm on acidification. Anal. Calcd for C16H18N4O4 : C, 58.17; H, 5.49; N, 16.96. Found: C, 57.81; H, 6.11; N, 16.84.

Source