HuagongsheHuagongshe Chemistry Print Report · For research reference only
8-Bromooctanamide → (7-Carbamoyl-heptyl)-{2-[(3,5-diamino-6-chloro-pyrazine-2-carbonyl)-amino]-ethyl}-dimethyl-ammonium bromide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 8-Bromooctanamide | HCID 13111846 | — |
| Reactant | 3,5-Diamino-6-chloro-N-[2-(dimethylamino)ethyl]-2-pyrazinecarboxamide | HCID 15148130 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | (7-Carbamoyl-heptyl)-{2-[(3,5-diamino-6-chloro-pyrazine-2-carbonyl)-amino]-ethyl}-dimethyl-ammonium bromide | HCID 86656654 | — |
Reaction Steps
A solution of 3,5-Diamino-6-chloro-pyrazine-2-carboxylic acid (2-dimethylamino-ethyl)-amide (Intermediate H) (100 mg, 0.39 mmol) and 8-Bromo-octanoic acid amide (Intermediate P) (130 mg, 0.6 mmol) in DMF (3 mL) is heated at 70° C. for 3 days. After this time, the solvent is removed in vacuo to yield an orange oil, which is triturated with acetone (2×10 mL) to afford the title compound. M+ 400.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08236808B2 |
| Source dataset | uspto-grants-2012_08 |
| ORD ID | ord-4067908afc0f42eaacf397e777483795 |
| Source note | uspto-grants-2012_08 |