Water → N'-(3-cyano-5-iodopyrazin-2-yl)-N,N-dimethylformimidamide

HRID 1048748

Reaction equation

HRID 1048748 reaction equation
P(Cl)(Cl)(Cl)=O.[NH2:6][C:7]1[C:8]([C:14]([NH2:16])=O)=[N:9][C:10]([I:13])=[CH:11][N:12]=1.O.[CH3:18][N:19]([CH3:22])[CH:20]=O>>[C:14]([C:8]1[C:7]([N:6]=[CH:18][N:19]([CH3:22])[CH3:20])=[N:12][CH:11]=[C:10]([I:13])[N:9]=1)#[N:16]

Participants

5

Procedure

13.59 ml (146 mmol) of phosphorus oxychloride is added drop by drop at 0° C. to 11 g (41.7 mmol) of a solution of 3-amino-6-iodopyrazine-2-carboxamide in 80 ml of dimethylformamide. The reaction mixture is stirred at room temperature overnight and then poured in a beaker containing ice and a little water. The pH is adjusted to 8 with 1 N soda solution; a precipitate is formed. The mixture is allowed to gradually return to room temperature and then the solid formed is filtered, rinsed with water and dried at 50° C. to yield 10.50 g of N′-(3-cyano-5-iodopyrazine-2-yl)-N,N-dimethyl formimidamide (84%) in the form of a beige solid.

Workup

  1. additionpoured in a beaker
  2. additioncontaining ice
  3. customa precipitate is formed
  4. customto gradually return to room temperature
  5. customthe solid formed
  6. filtrationis filtered
  7. washrinsed with water
  8. customdried at 50° C.

Sources & evidence

ORD record
ord-7b85590db64b43c99258225f17f9c21e
Source dataset
uspto-grants-2016_07
Patent number
US09381195B2

Linked notes

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