HuagongsheHuagongshe Chemistry Print Report · For research reference only
2-Amino-5-chloronicotinamide → 1-[3-(Aminocarbonyl)-5-chlorobenzyl]-5-chloro-2-imino-1,2-dihydropyridine-3-carboxamide hydrobromide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 2-Amino-5-chloronicotinamide | HCID 66876883 | — |
| Reactant | 3-(Bromomethyl)-5-chlorobenzamide | HCID 68661645 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | 1-[3-(Aminocarbonyl)-5-chlorobenzyl]-5-chloro-2-imino-1,2-dihydropyridine-3-carboxamide hydrobromide | HCID 68662045 | 30% |
Reaction Conditions
| Temperature | 100 °C |
|---|
Reaction Steps
(Step 3) To a solution of 2-amino-5-chloronicotinamide (0.15 g) in N,N-dimethylformamide (3 ml) was added 3-(bromomethyl)-5-chlorobenzamide (0.26 g) obtained in Step 2, and the mixture was stirred at 100° C. for 3 hr. The reaction mixture was diluted with ethyl acetate. The precipitate was collected by filtration and washed with ethyl acetate. The obtained precipitate was recrystallized from methanol-ethyl acetate to give the title compound (110 mg).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08470859B2 |
| Source dataset | uspto-grants-2013_06 |
| ORD ID | ord-dd7924e3a7564cf6a95896ac8fea6de4 |
| Source note | uspto-grants-2013_06 |