HuagongsheHuagongshe Chemistry Print Report · For research reference only
Oxalyl chloride → N-(6-Amino-5-chloropyrazin-2-yl)-5-methylisoxazole-4-carboxamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Oxalyl chloride | HCID 65578 | — |
| Reactant | 5-Methylisoxazole-4-carboxylic acid | HCID 1425240 | — |
| Reactant | 3-Chloropyrazine-2,6-diamine | HCID 12101492 | — |
| Catalyst | Dimethylformamide | HCID 6228 | — |
| Solvent | Pyridine | HCID 1049 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | N-(6-Amino-5-chloropyrazin-2-yl)-5-methylisoxazole-4-carboxamide | HCID 57799133 | 30.9% |
Reaction Steps
Oxalyl chloride (0.8 ml, 10.3 mmol) was added to a solution of 5-Methyl-isoxazole-4-carboxylic acid (1 g, 6.9 mmol) in dichloromethane (30 ml) followed by 1 drop of dimethylformamide. The mixture was stirred at room temperature for 5 hours before concentrating in vacuo and azeotroping with dichloromethane. The residue was taken up in pyridine (3 ml) and added to a solution of 3-chloro-pyrazine-2,6-diamine (Preparation 1) (0.65 g, 4.6 mmol) in anhydrous pyridine (30 ml) and the mixture heated at 50° C. for 3 hours before cooling to room temperature and concentrating in vacuo. The residue was purified by silica gel column chromatography, eluting with ethyl acetate:heptane 1:1, to afford the product as a white solid (360 mg).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07572797B2 |
| Source dataset | uspto-grants-2009_08 |
| ORD ID | ord-fcc19f1786764a93854115dbf73ab113 |
| Source note | uspto-grants-2009_08 |