HCID 19349406, compound → HCID 19349411, compound

HRID 1636809Notes

Reaction equation

HRID 1636809 reaction equation
[CH3:1][C:2]([C:6]1[CH:11]=[C:10]([CH2:12][N:13]2[CH:17]=[N:16][CH:15]=[N:14]2)[CH:9]=[C:8]([CH2:18][S:19][CH3:20])[CH:7]=1)([CH3:5])[C:3]#[N:4].I([O-])(=O)(=O)=[O:22].[Na+]>CO.O1CCCC1.O>[CH3:5][C:2]([C:6]1[CH:11]=[C:10]([CH2:12][N:13]2[CH:17]=[N:16][CH:15]=[N:14]2)[CH:9]=[C:8]([CH2:18][S:19]([CH3:20])=[O:22])[CH:7]=1)([CH3:1])[C:3]#[N:4]

Participants

6

Procedure

A solution of the product of Example 30 (0.16 g) in methanol (0.5 ml) and tetrahydrofuran (5 ml) was stirred while a solution of sodium periodate (0.15 g) in water (0.5 ml) was added, and was then stirred at room temperature for a further 18 h. Water (5 ml) was added and the mixture was extracted six times with dichloromethane. The extracts were combined, dried and evaporated to dryness, and the residue was purified by flash column chromatography, eluting with methanol:ethyl acetate (1:9 by volume) to give 2-methyl-2-[3-methylsulphinylmethyl-5-(1H-1,2,4-triazol-1-ylmethyl)phenyl]-propiononitrile. Nmr in deuteriochloroform; δ 8.16(1H,s), 8.0(1H,s), 7.38(1H,m), 7.27(1H,m), 7.15(1H,m), 5.4(2H,s), 3.98(1H,d), 3.88(1H,d), 2.5(3H,s), 1.72(6H,s).

Workup

  1. additionwas added
  2. extractionthe mixture was extracted six times with dichloromethane
  3. customdried
  4. customevaporated to dryness
  5. customthe residue was purified by flash column chromatography
  6. washeluting with methanol:ethyl acetate (1:9 by volume)

Sources & evidence

ORD record
ord-5255516c3b1747bb96080086d6ec9a46
Source dataset
uspto-grants-2000_03
Patent number
USRE036617

Reaction notes

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