Hydrochloric Acid → HCID 178510584, compound

HRID 2043798Notes

Reaction equation

HRID 2043798 reaction equation
C1(C)C=CC=CC=1.F[C:9]1[C:10]([C:16]#[N:17])=[N:11][C:12]([F:15])=[CH:13][N:14]=1.C([O-])(=[O:20])C.[Na+].Cl>C(OCC)(=O)C.O.CS(C)=O>[F:15][C:12]1[N:11]=[C:10]([C:16]#[N:17])[C:9]([OH:20])=[N:14][CH:13]=1

Participants

8

Conditions

Temperature
50 °C

Procedure

To 19.92 g of a toluene solution of 3,6-difluoropyrazine-2-carbonitrile with a concentration of 12.7% were sequentially added 18 ml of dimethyl sulfoxide, 9 ml of water, and 2.95 g of sodium acetate. The resulting mixture was heated to 50° C., and stirred at 50° C. for 7 hours. The mixture was then cooled to room temperature, and 9 ml of water and concentrated hydrochloric acid were added to adjust the pH to 2.5. 54 ml of ethyl acetate was added and a separation was performed. The separated organic layer was washed with 18 ml of water, and then washed with a 10% saline solution. Each of the aqueous layers was extracted with 18 ml of ethyl acetate, and the thus obtained organic layers were combined with the original organic layer. The ethyl acetate was then removed by distillation under reduced pressure, yielding 3.45 g of an oily 6-fluoro-3-hydroxypyrazine-2-carbonitrile.

Workup

  1. temperatureThe mixture was then cooled to room temperature
  2. customa separation
  3. washThe separated organic layer was washed with 18 ml of water
  4. washwashed with a 10% saline solution
  5. extractionEach of the aqueous layers was extracted with 18 ml of ethyl acetate
  6. customThe ethyl acetate was then removed by distillation under reduced pressure

Sources & evidence

ORD record
ord-274fecd5c927474489ad00dfb3a11b89
Source dataset
uspto-grants-2013_11
Patent number
US08586741B2

Reaction notes

Loading…