HuagongsheHuagongshe Chemistry Print Report · For research reference only
2-hydrazinyl-1H-1,3-benzodiazole → 1-(4-Pyrimidinyl)-1-ethanone-1-(1H-benzo[d]imidazol-2-yl)-hydrazone
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 2-hydrazinyl-1H-1,3-benzodiazole | HCID 95788 | — |
| Reactant | 1-(Pyrimidin-4-yl)ethanone | HCID 538060 | — |
| Catalyst | Acetic Acid | HCID 176 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | 1-(4-Pyrimidinyl)-1-ethanone-1-(1H-benzo[d]imidazol-2-yl)-hydrazone | HCID 396596 | — |
Reaction Steps
A mixture of 4-acetyl pyrimidine (0.412 g, 3.37 mmol) and 2-hydrazinobenzimidazole (0.50 g, 3.37 mmol) in 15 ml of methanol is refluxed after the addition of 5 drops of glacial acetic acid, until monitoring of the reaction by means of thin layer chromatography (Polygram Sil G/UV254 prefabricated foils; eluting agent: CH2Cl2:MeOH (10:1)) did not reveal any further reaction. The reaction mixture is stored over night in the refrigerator at approximately 5° C. The precipitate is filtered and recrystallized from a mixture of ethyl acetate and diisopropyl ether. Yield: 0.65 g (76% of theory).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07112680B2 |
| Source dataset | uspto-grants-2006_09 |
| ORD ID | ord-5240fdcc2ced43c694813d50576c545a |
| Source note | uspto-grants-2006_09 |