Sodium Nitrite → HCID 54569597, compound

HRID 2083783Notes

Reaction equation

HRID 2083783 reaction equation
[C@@H:1]1([NH:12][C:13]([NH:15][CH3:16])=[O:14])[O:9][C@H:8]([CH2:10][OH:11])[C@@H:6]([OH:7])[C@H:4]([OH:5])[C@@H:2]1[OH:3].[N:17]([O-])=[O:18].[Na+]>C(O)(=O)C.O>[C@@H:1]1([NH:12][C:13]([N:15]([CH3:16])[N:17]=[O:18])=[O:14])[O:9][C@H:8]([CH2:10][OH:11])[C@@H:6]([OH:7])[C@H:4]([OH:5])[C@@H:2]1[OH:3]

Participants

5

Procedure

1-(β-D-mannopyranosyl)-3-methyl-urea (200 mg) was dissolved in a mixture of 1.5 ml of glacial acetic acid and 3.5 ml of water, and the resulting solution was admixed with 99 mg of sodium nitrite. The mixture so obtained was agitated for 3 hours at ambient temperature to effect the nitrosation. The reaction mixture was treated with Amberlite IR-120 (H+ form) to remove sodium cation therefrom. The reaction mixture so treated was then concentrated by distillation under reduced pressure at a temperature of less than 30° C to remove the solvent, so that a crystalline product was deposited. This crystalline product was collected by filtration and washed with n-propanol, affording 180 mg of the titled compound. Yield 78%. mp. 103° C (with decomposition). [α]D26 -12.6° (c 0.99, H2O).

Workup

  1. customThe mixture so obtained
  2. additionThe reaction mixture was treated with Amberlite IR-120 (H+ form)
  3. customto remove sodium cation
  4. additionThe reaction mixture so treated
  5. concentrationwas then concentrated by distillation under reduced pressure at a temperature of less than 30° C
  6. customto remove the solvent
  7. filtrationThis crystalline product was collected by filtration
  8. washwashed with n-propanol

Sources & evidence

ORD record
ord-f2f438a5ae0d4b3699f0d269006d9602
Source dataset
uspto-grants-1978_04
Patent number
US04086415

Reaction notes

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