HuagongsheHuagongshe Chemistry Print Report · For research reference only
Hydrazine → HCID 178456320, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Hydrazine | HCID 9321 | — |
| Reactant | 1,4-Dichloro-2-butyne | HCID 13182 | — |
| Reactant | Hydrogen iodide | HCID 24841 | — |
| Reactant | Sodium | HCID 5360545 | — |
| Reactant | N-(4-(1H-imidazol-1yl)2-butyn-1-yl)phthalimide | HCID 13588985 | — |
| Reactant | 2-Methylthiobenz(cd)indole hydriodide | HCID 20150650 | — |
| Reactant | Phthalimide potassium salt | HCID 24194345 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 178456320 | HCID 178456320 | — |
Reaction Steps
The sequential reaction of 1,4-dichloro-2-butyne with potassium phthalimide and then the sodium salt of imidazole leads to the formation of N-(4-(1H-imidazol-1yl)2-butyn-1-yl)phthalimide, which upon treatment with hydrazine in boiling ethanol leads to 4-(1H-imidazol-lyl)-2-butyn-1-ylamine. Reaction of the latter compound with 2-methylthiobenz(cd)indole hydriodide in ethanol solution, by the conditions of Example 52 leads to the hydriodide of the title compound which is converted to the free base by treatment with alkali hydroxide solution.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05081131 |
| Source dataset | uspto-grants-1992_01 |
| ORD ID | ord-e2d1154b877b45d5baf2b48acffe8064 |
| Source note | uspto-grants-1992_01 |