HuagongsheHuagongshe Chemistry Print Report · For research reference only
Toluene → N'-(2-chlorocyclohexyl)-urea
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Toluene | HCID 1140 | — |
| Reactant | N-(aminocarbonyl)benzenesulphonamide | HCID 118791 | — |
| Reactant | 2-Chlorocyclohexan-1-amine | HCID 418800 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Product | N'-(2-chlorocyclohexyl)-urea | HCID 85911145 | — |
Reaction Steps
A mixture of 10.3 g of of N-[4-<2-methoxy-5-chlorobenzamido>-ethyl)-benzenesulfonyl]-ethyl)-benzenesulfonyl-urea (melting point 171° -173°C), 300 ml of toluene, 30 ml of glycolmonomethyl-ether, 1.65 g of glacial acetic acid and 3.3 g of 2-chloro-cyclohexylamine are heated under reflux for 5 hours. Then the whole is concentrated in vacuo and the residue is treated with alcohol. The N-[4-(β<2-methoxy-5-chlorobenzamido> -ethyl)-benzenesulfonyl]-N'-(2-chlorocyclohexyl)-urea obtained as crude product melts at 194° -195°C after recrystallization from methanol/dimethylformamide.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US03932503 |
| Source dataset | uspto-grants-1976_01 |
| ORD ID | ord-2336f2a4baa044938270d14e125c5e92 |
| Source note | uspto-grants-1976_01 |