HuagongsheHuagongshe Chemistry Print Report · For research reference only
Clonidine → 2-[N-(2,6-dichlorophenyl)-N-(2-methyl-1-butene-4-yl)-amino]2-imidazoline
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Clonidine | HCID 2803 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 4-Bromo-2-methylbut-1-ene | HCID 549585 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | 2-[N-(2,6-dichlorophenyl)-N-(2-methyl-1-butene-4-yl)-amino]2-imidazoline | HCID 23454107 | — |
Reaction Conditions
| Temperature | 120 °C |
|---|
Reaction Steps
A mixture of 6.9 gm (0.03 mol) of clonidine, 5.6 gm of 4-bromo-2-methyl-1-butene, and 5 ml of triethylamine in 25 ml of toluene was heated for 24 hours at 120° C. After cooling, the solvent was decanted, and the residue remaining was dissolved in 1 N hydrochloric acid. After extraction with ether several times (the ethereal extracts were abandoned), the solution was extracted with ether in fractions at stepwisely rising pH values (alkalizing with 2 N sodium hydroxide solution). The thin-layer chromatographically uniform ether extracts were united and dried over MgSO4, and the ether was evaporated in vacuo.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04277487 |
| Source dataset | uspto-grants-1981_07 |
| ORD ID | ord-3d87352bb14d48abb106dbb312628568 |
| Source note | uspto-grants-1981_07 |