HuagongsheHuagongshe Chemistry Print Report · For research reference only
Dimethylformamide → HCID 13344910, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Dimethylformamide | HCID 6228 | — |
| Reactant | Ethyl Acetate | HCID 8857 | — |
| Reactant | Cyanogen Bromide | HCID 10476 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 1-[2-(2-Imidazolylmethyl) phenylthiocarbamoyl]-4-methylpiperazine | HCID 20403308 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | HCID 13344910 | HCID 13344910 | — |
Reaction Steps
The mixture of 315 mg of 1-[2-(2-imidazolylmethyl) phenylthiocarbamoyl]-4-methylpiperazine, 3.3 ml of dimethylformamide, 276 mg of potassium carbonate, 116 mg of cyanogen bromide and 50 mg of 8-crown-6 ether is stirred at room temperature under nitrogen for 3 hours. It is diluted with ethyl acetate, washed with saturated aqueous sodium chloride, dried and evaporated. The residue is dissolved in acetone, the solution treated with 116 mg of maleic acid and diluted with diethyl ether, to yield 5-(4-methyl-1-piperazinyl)-11H-imidazo[1,2-c]-[1,3] benzodiazepine monomaleate of example 1.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04460587 |
| Source dataset | uspto-grants-1984_07 |
| ORD ID | ord-3b9517b45ba144ddb1a26f89fef80863 |
| Source note | uspto-grants-1984_07 |