HuagongsheHuagongshe Chemistry Print Report · For research reference only
Dimethylformamide → 2,3-Dihydro-3-(4-ethoxycarbonylbut-1-yl)-4-methyl-2-oxo-1-pyrid-3-ylmethyleneamino-1H-imidazole
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Dimethylformamide | HCID 6228 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | 2,3-Dihydro4-methyl-2-oxo-1-pyrid-3-ylmethyleneamino-1H-imidazole | HCID 54124030 | — |
| Reactant | 1-Bromo-4-ethoxy-carbonyl-butane | HCID 86751414 | — |
| Product | 2,3-Dihydro-3-(4-ethoxycarbonylbut-1-yl)-4-methyl-2-oxo-1-pyrid-3-ylmethyleneamino-1H-imidazole | HCID 70338013 | — |
Reaction Steps
0.72 g of sodium hydride are added to a suspension of 4.1 g of 2,3-dihydro-4-methyl-2-oxo-1-pyrid-3-ylmethyleneamino-1H-imidazole in 80 ml of N,N-dimethylformamide. The mixture is heated to 50°, treated with a solution of 5.22 g of 1-bromo-4-ethoxy-carbonyl-butane in 20 ml of N,N-dimethylformamide, and stirred for 30 minutes. The N,N-dimethylformamide is then removed on a rotary evaporator. The residue is treated with ethyl acetate, during which process sodium bromide precipitates. The mixture is filtered over Celite, and the filtrate is evaporated. The residue is treated with hexane, during which process crystals precipitate. The crystals are filtered off with suction and dried yielding the title compound melting at 74°-76°.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05679623 |
| Source dataset | uspto-grants-1997_10 |
| ORD ID | ord-9f87968347104a21b315c9bcbb925c1d |
| Source note | uspto-grants-1997_10 |