HuagongsheHuagongshe Chemistry Print Report · For research reference only
Benzene → N-{4-[2-(1H-Indol-3-yl)ethyl]piperazin-1-yl}-N'-phenylurea
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Benzene | HCID 241 | — |
| Reactant | Phenyl isocyanate | HCID 7672 | — |
| Reactant | HCID 12392200 | HCID 12392200 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | N-{4-[2-(1H-Indol-3-yl)ethyl]piperazin-1-yl}-N'-phenylurea | HCID 12464884 | — |
Reaction Steps
A stirred solution of 6.13 g of 3-[2-(4-aminopiperazin-1-yl)ethyl]indole and 3.53 g of phenylisocyanate in 100 ml. of dry benzene is refluxed for 6 hours and then allowed to stand at ambient temperature overnight. Ether is added slowly to promote crystallization. The solid product is filtered, washed with ether and dried. The solid is recrystallized twice from a dimethylformamide water mixture to give crystals m.p. 168°-171° C. of 1-[1-(indol-3-ylethyl)piperazin-4-yl]-3-phenylurea.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04024258 |
| Source dataset | uspto-grants-1977_05 |
| ORD ID | ord-1091fe74057547689aaad3f9ee05d6f0 |
| Source note | uspto-grants-1977_05 |