Sodium periodate → HCID 59432143, compound

HRID 506472Notes

Reaction equation

HRID 506472 reaction equation
[CH3:1][O:2][C:3]([C:5]1[C:10]([CH:11]=C)=[C:9]([NH2:13])[N:8]=[C:7]([C:14]2[CH:19]=[CH:18][C:17]([Cl:20])=[C:16]([O:21][CH3:22])[C:15]=2[F:23])[N:6]=1)=[O:4].I([O-])(=O)(=O)=[O:25].[Na+]>C1COCC1.O.[Os](=O)(=O)(=O)=O>[CH3:1][O:2][C:3]([C:5]1[C:10]([CH:11]=[O:25])=[C:9]([NH2:13])[N:8]=[C:7]([C:14]2[CH:19]=[CH:18][C:17]([Cl:20])=[C:16]([O:21][CH3:22])[C:15]=2[F:23])[N:6]=1)=[O:4]

Participants

6

Procedure

6-Amino-2-(4-chloro-2-fluoro-3-methoxyphenyl)-5-vinyl-pyrimidine-4-carboxylic acid methyl ester (0.500 g, 1.5 mmol) was dissolved in THF (3 mL) and water (3 mL). Osmium tetroxide (4 mg, 0.015 mmol) was added and the reaction mixture was stirred for 2 min. Sodium periodate (0.63 g, 3 mmol) was then added over a period of 2 min. The reaction mixture was stirred for 16 h at ambient temperature then poured into water (150 mL) and extracted with dichloromethane thrice. The combined organic layers were dried, filtered and concentrated to afford the title compound (490 mg, 98% yield) in sufficient purity for subsequent reactions. An analytical sample was obtained by reverse phase chromatography: 1H NMR (CDCl3) δ 10.31 (s, 1H), 8.72 (br s, 1H), 7.77 (dd, 1H), 7.23 (m, 1H), 6.03 (br s, 1H), 4.06 (s, 3H), 4.01 (d, 3H).

Workup

  1. stirringThe reaction mixture was stirred for 16 h at ambient temperature
  2. extractionextracted with dichloromethane thrice
  3. customThe combined organic layers were dried
  4. filtrationfiltered
  5. concentrationconcentrated

Sources & evidence

ORD record
ord-a1bdd939bf604d399786b44d3533483f
Source dataset
uspto-grants-2010_08
Patent number
US07786044B2

Reaction notes

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