HuagongsheHuagongshe Chemistry Print Report · For research reference only
Benzoyl chloride → N-(pyrazin-2-ylcarbamothioyl)benzamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Benzoyl chloride | HCID 7412 | — |
| Reactant | Ammonium thiocyanate | HCID 15666 | — |
| Reactant | Aminopyrazine | HCID 78747 | — |
| Solvent | Acetone | HCID 180 | — |
| Product | N-(pyrazin-2-ylcarbamothioyl)benzamide | HCID 14460677 | — |
Reaction Steps
To a solution of ammonium thiocyanate (17.8 g, 0.234 mol) in dry acetone (200 ml) at 0° C. under nitrogen is added benzoyl chloride (30 g, 0.213 mol) slowly over a period of 15 min. The reaction mixture is stirred at room temperature for 30min and filtered. To the filtrate is added 2-amino pyrazine (16.2 g, 0.17 mol) dropwise and stirred for 3 h at room temperature. The solvent is removed under vacuum and the residue is diluted with water. The solid precipitated is filtered and dried to afford N-[(pyrazin-2-ylamino)carbonothioyl]benzamide as a solid (33 g; 76%). TLC—Chloroform/methanol (9/1): Rf−0.5.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07799814B2 |
| Source dataset | uspto-grants-2010_09 |
| ORD ID | ord-727f384ed81049c39d2257d227129f1a |
| Source note | uspto-grants-2010_09 |