HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethanol → 1-{3-[4-(4-Chlorobenzyl)piperazin-1-yl]propyl}-3-phenylurea
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethanol | HCID 702 | — |
| Reactant | Phenyl isocyanate | HCID 7672 | — |
| Reactant | HCID 13606667 | HCID 13606667 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 1-{3-[4-(4-Chlorobenzyl)piperazin-1-yl]propyl}-3-phenylurea | HCID 13606678 | 21.4% |
Reaction Steps
A solution of 1-(3-aminopropyl)-4-(4-chlorobenzyl)piperazine (2.0 g; 7.5 mmole) and phenyl isocyanate (1.6 g; 13.4 mmole) in tetrahydrofuran (5 ml) was stirred at room temperature for 30 minutes. Ethanol (5 ml) was added, and the reaction mixture was stirred for 3 hours and then concentrated under reduced pressure. The residue was crystallized from aqueous ethanol to provide crude product (2.7 g). Recrystallization from the same solvent yielded the title compound as colorless crystals (0.62 g; 21% yield), m.p. 135°-137° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04579947 |
| Source dataset | uspto-grants-1986_04 |
| ORD ID | ord-d61f9f2102da41b6a46ba3319715bac8 |
| Source note | uspto-grants-1986_04 |