HCID 18007943, compound → HCID 18007946, compound

HRID 988224Notes

Reaction equation

HRID 988224 reaction equation
I([O-])(=O)(=O)=[O:2].[Na+].[CH:7]([C:9]1[CH:10]=[CH:11][C:12]2[S:16][CH:15]=[C:14]([CH2:17][CH2:18][NH:19][C:20]([CH:22]3[CH2:27][CH2:26][CH2:25][CH2:24][CH2:23]3)=[O:21])[C:13]=2[CH:28]=1)=C>CC(O)(C)C.O1CCOCC1.O.[Os](=O)(=O)(=O)=O>[CH:7]([C:9]1[CH:10]=[CH:11][C:12]2[S:16][CH:15]=[C:14]([CH2:17][CH2:18][NH:19][C:20]([CH:22]3[CH2:27][CH2:26][CH2:25][CH2:24][CH2:23]3)=[O:21])[C:13]=2[CH:28]=1)=[O:2]

Participants

7

Procedure

1.10 g of osmium tetroxide in 2-methyl-2-propanol and then 8.70 g of sodium periodate are added at room temperature to a solution of 10 mmol of the product obtained in Step D in a mixture of 50 ml of dioxane and 25 ml of water. After stirring overnight at room temperature, the suspension is filtered and the filtrate is concentrated under reduced pressure. The resulting residue is taken up in dichloromethane. The organic phase is washed with water, dried and evaporated. The residue is purified by chromatography over silica gel to yield the title product.

Workup

  1. filtrationthe suspension is filtered
  2. concentrationthe filtrate is concentrated under reduced pressure
  3. washThe organic phase is washed with water
  4. customdried
  5. customevaporated
  6. customThe residue is purified by chromatography over silica gel

Sources & evidence

ORD record
ord-ec3c3c5022ab4736b16a8c0a004f688b
Source dataset
uspto-grants-2003_10
Patent number
US06635650B2

Reaction notes

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