HuagongsheHuagongshe Chemistry Print Report · For research reference only
Methyl iodide → {2-[(3,5-Diamino-6-chloro-pyrazine-2-carbonyl)-amino]-ethyl}-trimethyl-ammonium iodide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Methyl iodide | HCID 6328 | — |
| Reactant | 3,5-Diamino-6-chloro-N-[2-(dimethylamino)ethyl]-2-pyrazinecarboxamide | HCID 15148130 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | {2-[(3,5-Diamino-6-chloro-pyrazine-2-carbonyl)-amino]-ethyl}-trimethyl-ammonium iodide | HCID 57400252 | — |
Reaction Steps
Methyl iodide (120 μL, 1.9 mmol) is added to a suspension of 3,5-Diamino-6-chloro-pyrazine-2-carboxylic acid (2-dimethylamino-ethyl)-amide (Intermediate H) (100 mg, 0.39 mmol) in DCM (4 mL), and the resultant solution is stirred at RT for 2 h. The white solid which has formed is collected by filtration and washed with DCM (5 mL) to afford the title compound. M+ 273. 1H NMR (400 MHz, DMSO-d6) δ 8.27 (1H, t), 7.09 (2H, br s), 3.61 (2H, m), 3.45 (2H, t), 3.11 (9H, s).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08236808B2 |
| Source dataset | uspto-grants-2012_08 |
| ORD ID | ord-8a78244253744e2eb3492991cbe6b00c |
| Source note | uspto-grants-2012_08 |