HuagongsheHuagongshe Chemistry Print Report · For research reference only
Water → N'-(3-cyano-5-iodopyrazin-2-yl)-N,N-dimethylformimidamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Dimethylformamide | HCID 6228 | — |
| Reactant | Phosphorus oxychloride | HCID 24813 | — |
| Reactant | 3-Amino-6-iodopyrazine-2-carboxamide | HCID 46863952 | — |
| Product | N'-(3-cyano-5-iodopyrazin-2-yl)-N,N-dimethylformimidamide | HCID 86680553 | 84% |
Reaction Steps
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.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08883821B2 |
| Source dataset | uspto-grants-2014_11 |
| ORD ID | ord-8e059d6ea9a041a5b2e2fb4d7888fcb8 |
| Source note | uspto-grants-2014_11 |