HuagongsheHuagongshe Chemistry Print Report · For research reference only
Dichloromethane → 3-Aminopyrazine-2-carboxylic acid 2-chlorophenylamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Dichloromethane | HCID 6344 | — |
| Reactant | 2-Chloroaniline | HCID 7240 | — |
| Reactant | 3-Amino-2-pyrazinecarboxylic acid | HCID 72656 | — |
| Reactant | 1,3-Propanediamine, N'-(ethylcarbonimidoyl)-N,N-dimethyl-, monohydrochloride | HCID 2723939 | — |
| Catalyst | 4-(Dimethylamino)pyridine | HCID 14284 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 3-Aminopyrazine-2-carboxylic acid 2-chlorophenylamide | HCID 54096972 | 50% |
Reaction Steps
A mixture of 3-aminopyrazine carboxylic acid (7.0 g, 50.32 mmol), methylene chloride (60 mL), dimethylformamide (40 mL), 4-dimethylaminopyridine (15.37 g, 126 mmol), 2-chloroaniline (5.82 mL, 55.35 mmol), and 1-(3-dimethylaminopropyl)-3-ethylcarbodiimide hydrochloride (11.58 g, 60.38 mmol) was stirred overnight at ambient temperature. The solvent was removed and the residue was mixed with ethyl acetate and 1 N lithium chloride. The precipitate which formed was filtered and rinsed with 1 N lithium chloride, ethyl acetate, and ether and then air dried to afford 6.22 g (50%) of 3-aminopyrazine-2-carboxylic acid 2-chlorophenylamide as fluffy yellow crystals.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06323208B1 |
| Source dataset | uspto-grants-2001_11 |
| ORD ID | ord-6896b7fd7f444ab7bda70b4c478c1ee7 |
| Source note | uspto-grants-2001_11 |