HuagongsheHuagongshe Chemistry Print Report · For research reference only
Chloroacetonitrile → 3-Cyanomethyl-2,3-dihydro-4-methyl-2-oxo-1-pyrid-3-ylmethyleneamino-1H-imidazole
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Chloroacetonitrile | HCID 7856 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | 2,3-Dihydro4-methyl-2-oxo-1-pyrid-3-ylmethyleneamino-1H-imidazole | HCID 54124030 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 3-Cyanomethyl-2,3-dihydro-4-methyl-2-oxo-1-pyrid-3-ylmethyleneamino-1H-imidazole | HCID 86751413 | — |
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 1.89 g of chloroacetonitrile in 20 ml of N,N-dimethylformamide, and stirred for 30 minutes. The N,N-dimethylformamide is then removed on a rotary evaporator. In a mixer, the residue is mixed intimately with water. The crystals are filtered off, yielding the title compound melting at 195°-198°.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05679623 |
| Source dataset | uspto-grants-1997_10 |
| ORD ID | ord-7d31497fca674e108d78873ec29a352a |
| Source note | uspto-grants-1997_10 |